Canonical Allele Identifier: CA449791367
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31357352-T-C
MyVariant Identifiers: chr6:g.31325129T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357352T>C , CM000668.2:g.31357352T>C GRCh38
NC_000006.11:g.31325129T>C , CM000668.1:g.31325129T>C GRCh37
NC_000006.10:g.31433108T>C NCBI36
NG_023187.1:g.4861A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1339-59A>G
ENST00000481849.6:n.1339-59A>G
ENST00000497377.6:n.1339-59A>G
ENST00000696559.1:c.-135-59A>G ENSP00000512717.1:n.-135-59A>G
ENST00000696560.1:c.-135-59A>G ENSP00000512718.1:n.-135-59A>G
ENST00000696561.1:c.-135-59A>G ENSP00000512719.1:n.-135-59A>G
ENST00000696562.1:c.-135-59A>G ENSP00000512720.1:n.-135-59A>G
ENST00000603274.1:n.706T>C
XR_926692.1:n.165-59A>G
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