Canonical Allele Identifier: CA449791045
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v4: 6-31357238-T-A
MyVariant Identifiers: chr6:g.31325015T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357238T>A , CM000668.2:g.31357238T>A GRCh38
NC_000006.11:g.31325015T>A , CM000668.1:g.31325015T>A GRCh37
NC_000006.10:g.31432994T>A NCBI36
NG_023187.1:g.4975A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1394A>T
ENST00000481849.6:n.1394A>T
ENST00000497377.6:n.1394A>T
ENST00000696559.1:c.-80A>T ENSP00000512717.1:n.-80A>T
ENST00000696560.1:c.-80A>T ENSP00000512718.1:n.-80A>T
ENST00000696561.1:c.-80A>T ENSP00000512719.1:n.-80A>T
ENST00000696562.1:c.-80A>T ENSP00000512720.1:n.-80A>T
ENST00000603274.1:n.592T>A
NM_005514.7:c.-80A>T NP_005505.2:n.-80A>T