Canonical Allele Identifier: CA136837278
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs564170445
gnomAD v2: 6-31327058-G-A
gnomAD v3: 6-31359281-G-A
gnomAD v4: 6-31359281-G-A
MyVariant Identifiers: chr6:g.31327058G>A (hg19) chr6:g.31359281G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31359281G>A , CM000668.2:g.31359281G>A GRCh38
NC_000006.11:g.31327058G>A , CM000668.1:g.31327058G>A GRCh37
NC_000006.10:g.31435037G>A NCBI36
NG_023187.1:g.2932C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1271-1600C>T
ENST00000481849.6:n.1271-1600C>T
ENST00000497377.6:n.1271-1600C>T
ENST00000696559.1:c.-203-1600C>T ENSP00000512717.1:n.-203-1600C>T
ENST00000696560.1:c.-203-1600C>T ENSP00000512718.1:n.-203-1600C>T
ENST00000696561.1:c.-203-1600C>T ENSP00000512719.1:n.-203-1600C>T
ENST00000696562.1:c.-135-1988C>T ENSP00000512720.1:n.-135-1988C>T
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