Canonical Allele Identifier: CA449790858

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357172-G-A
• MyVariant Identifiers: chr6:g.31324949G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357172G>A , CM000668.2:g.31357172G>A	GRCh38
NC_000006.11:g.31324949G>A , CM000668.1:g.31324949G>A	GRCh37
NC_000006.10:g.31432928G>A	NCBI36
NG_023187.1:g.5041C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1460C>T
ENST00000481849.6:n.1460C>T
ENST00000497377.6:n.1460C>T
ENST00000696559.1:c.-14C>T	ENSP00000512717.1:n.-14C>T
ENST00000696560.1:c.-14C>T	ENSP00000512718.1:n.-14C>T
ENST00000696561.1:c.-14C>T	ENSP00000512719.1:n.-14C>T
ENST00000696562.1:c.-14C>T	ENSP00000512720.1:n.-14C>T
ENST00000412585.7:c.-14C>T MANE Select	ENSP00000399168.2:n.-14C>T
ENST00000412585.6:c.-14C>T	ENSP00000399168.2:n.-14C>T
ENST00000434333.1:c.-109C>T	ENSP00000405931.1:n.-109C>T
ENST00000498007.1:n.8C>T
ENST00000603274.1:n.526G>A
NM_005514.6:c.-14C>T	NP_005505.2:n.-14C>T
NM_005514.7:c.-14C>T	NP_005505.2:n.-14C>T
NM_005514.8:c.-14C>T MANE Select	NP_005505.2:n.-14C>T