ClinVar

NM_000392.5(ABCC2):c.577-3C>T

Gene:

ABCC2:ATP binding cassette subfamily C member 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q24.2

Genomic location:

• Chr10: 99794410 (on Assembly GRCh38)
• Chr10: 101554167 (on Assembly GRCh37)

Preferred name:

NM_000392.5(ABCC2):c.577-3C>T

HGVS:

• NC_000010.11:g.99794410C>T
• NG_011798.2:g.16813C>T
• NM_000392.5:c.577-3C>TMANE SELECT
• LRG_1208t1:c.577-3C>T
• LRG_1208:g.16813C>T
• NC_000010.10:g.101554167C>T
• NG_011798.1:g.16705C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs370534491

NCBI 1000 Genomes Browser:

rs370534491

Molecular consequence:

• NM_000392.5:c.577-3C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

2