Canonical Allele Identifier: CA136836859
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs560925699
gnomAD v2: 6-31325397-T-C
gnomAD v3: 6-31357620-T-C
gnomAD v4: 6-31357620-T-C
MyVariant Identifiers: chr6:g.31325397T>C (hg19) chr6:g.31357620T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357620T>C , CM000668.2:g.31357620T>C GRCh38
NC_000006.11:g.31325397T>C , CM000668.1:g.31325397T>C GRCh37
NC_000006.10:g.31433376T>C NCBI36
NG_023187.1:g.4593A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1332A>G
ENST00000481849.6:n.1332A>G
ENST00000497377.6:n.1332A>G
ENST00000696559.1:c.-142A>G ENSP00000512717.1:n.-142A>G
ENST00000696560.1:c.-142A>G ENSP00000512718.1:n.-142A>G
ENST00000696561.1:c.-142A>G ENSP00000512719.1:n.-142A>G
ENST00000696562.1:c.-135-327A>G ENSP00000512720.1:n.-135-327A>G
ENST00000603274.1:n.974T>C
XR_926692.1:n.158A>G
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