Canonical Allele Identifier: CA12291940
Gene: HLA-W HGNC NCBI

Linked Data

dbSNP Id: rs892666
gnomAD v2: 6-29924728-T-C
gnomAD v3: 6-29956951-T-C
gnomAD v4: 6-29956951-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29956951T>C , CM000668.2:g.29956951T>C GRCh38
NC_000006.11:g.29924728T>C , CM000668.1:g.29924728T>C GRCh37
NC_000006.10:g.30032707T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439514.1:n.261+95T>C