ClinVar

NM_000540.3(RYR1):c.4878C>T (p.Ala1626=)

Gene:

RYR1:ryanodine receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 38483460 (on Assembly GRCh38)
• Chr19: 38974100 (on Assembly GRCh37)

Preferred name:

NM_000540.3(RYR1):c.4878C>T (p.Ala1626=)

HGVS:

• NC_000019.10:g.38483460C>T
• NG_008866.1:g.54761C>T
• NM_000540.3:c.4878C>TMANE SELECT
• NM_001042723.2:c.4878C>T
• NP_000531.2:p.Ala1626=
• NP_000531.2:p.Ala1626=
• NP_001036188.1:p.Ala1626=
• LRG_766t1:c.4878C>T
• LRG_766:g.54761C>T
• LRG_766p1:p.Ala1626=
• NC_000019.9:g.38974100C>T
• NM_000540.2:c.4878C>T
• NP_000531.2:p.(=)

This HGVS expression did not pass validation

Links:

dbSNP: rs369466056

NCBI 1000 Genomes Browser:

rs369466056

Molecular consequence:

• NM_000540.3:c.4878C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001042723.2:c.4878C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

2