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Human Genome Region MHC

Assembly:
GRCh38
Location:
chr6:28,510,120-33,480,577
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL000250.2 NT_167244.2 ALT 4,672,374 6,441 16,129
GL000251.2 NT_113891.3 ALT 4,795,265 19,992 42,997
GL000252.2 NT_167245.2 ALT 4,604,811 15,386 93,609
GL000253.2 NT_167246.2 ALT 4,677,643 16,364 205,504
GL000254.2 NT_167247.2 ALT 4,827,813 12,868 82,650
GL000255.2 NT_167248.2 ALT 4,606,388 18,646 35,169
GL000256.2 NT_167249.2 ALT 4,929,269 16,203 199,106
KI270758.1 NT_187692.1 ALT 76,752 288 8,000
           

MHC -- chr6 (NC_000006.12):28,510,120-33,480,577