Canonical Allele Identifier: CA449791069
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs9266210
gnomAD v4: 6-31357246-T-G
MyVariant Identifiers: chr6:g.31325023T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357246T>G , CM000668.2:g.31357246T>G GRCh38
NC_000006.11:g.31325023T>G , CM000668.1:g.31325023T>G GRCh37
NC_000006.10:g.31433002T>G NCBI36
NG_023187.1:g.4967A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1386A>C
ENST00000481849.6:n.1386A>C
ENST00000497377.6:n.1386A>C
ENST00000696559.1:c.-88A>C ENSP00000512717.1:n.-88A>C
ENST00000696560.1:c.-88A>C ENSP00000512718.1:n.-88A>C
ENST00000696561.1:c.-88A>C ENSP00000512719.1:n.-88A>C
ENST00000696562.1:c.-88A>C ENSP00000512720.1:n.-88A>C
ENST00000603274.1:n.600T>G
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