Canonical Allele Identifier: CA449790888
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31357183-T-A
gnomAD v4: 6-31357183-T-A
MyVariant Identifiers: chr6:g.31324960T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357183T>A , CM000668.2:g.31357183T>A GRCh38
NC_000006.11:g.31324960T>A , CM000668.1:g.31324960T>A GRCh37
NC_000006.10:g.31432939T>A NCBI36
NG_023187.1:g.5030A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1449A>T
ENST00000481849.6:n.1449A>T
ENST00000497377.6:n.1449A>T
ENST00000696559.1:c.-25A>T ENSP00000512717.1:n.-25A>T
ENST00000696560.1:c.-25A>T ENSP00000512718.1:n.-25A>T
ENST00000696561.1:c.-25A>T ENSP00000512719.1:n.-25A>T
ENST00000696562.1:c.-25A>T ENSP00000512720.1:n.-25A>T
ENST00000412585.6:c.-25A>T ENSP00000399168.2:n.-25A>T
ENST00000434333.1:c.-120A>T ENSP00000405931.1:n.-120A>T
ENST00000603274.1:n.537T>A
NM_005514.6:c.-25A>T NP_005505.2:n.-25A>T
NM_005514.7:c.-25A>T NP_005505.2:n.-25A>T