Canonical Allele Identifier: CA12291940
Gene: HLA-W HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.29956951T>C
GRCh37 chr6:g.29924728T>C
gnomAD v2:
6:29924728 T / C
gnomAD v3:
6:29956951 T / C
gnomAD v4:
chr6-29956951-T-C
Joint Max Group AF 0.66591495 (NFE)
Genomes Max Group AF 0.66597513 (NFE)
Exomes Max Group AF 0.39402423 (NFE)
dbSNP:
892666
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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
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