Canonical Allele Identifier: CA449790854

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357170-A-T
• MyVariant Identifiers: chr6:g.31324947A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357170A>T , CM000668.2:g.31357170A>T	GRCh38
NC_000006.11:g.31324947A>T , CM000668.1:g.31324947A>T	GRCh37
NC_000006.10:g.31432926A>T	NCBI36
NG_023187.1:g.5043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1462T>A
ENST00000481849.6:n.1462T>A
ENST00000497377.6:n.1462T>A
ENST00000696559.1:c.-12T>A	ENSP00000512717.1:n.-12T>A
ENST00000696560.1:c.-12T>A	ENSP00000512718.1:n.-12T>A
ENST00000696561.1:c.-12T>A	ENSP00000512719.1:n.-12T>A
ENST00000696562.1:c.-12T>A	ENSP00000512720.1:n.-12T>A
ENST00000412585.7:c.-12T>A MANE Select	ENSP00000399168.2:n.-12T>A
ENST00000412585.6:c.-12T>A	ENSP00000399168.2:n.-12T>A
ENST00000434333.1:c.-107T>A	ENSP00000405931.1:n.-107T>A
ENST00000498007.1:n.10T>A
ENST00000603274.1:n.524A>T
NM_005514.6:c.-12T>A	NP_005505.2:n.-12T>A
NM_005514.7:c.-12T>A	NP_005505.2:n.-12T>A
NM_005514.8:c.-12T>A MANE Select	NP_005505.2:n.-12T>A