Canonical Allele Identifier: CA15453461

Gene: HLA-B

Linked Data

• dbSNP Id: rs1057387
• gnomAD v2: 6-31321753-T-G
• gnomAD v3: 6-31353976-T-G
• gnomAD v4: 6-31353976-T-G
• MyVariant Identifiers: chr6:g.31321753T>G (hg19) ; chr6:g.31353976T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353976T>G , CM000668.2:g.31353976T>G	GRCh38
NC_000006.11:g.31321753T>G , CM000668.1:g.31321753T>G	GRCh37
NC_000006.10:g.31429732T>G	NCBI36
NG_023187.1:g.8237A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3461A>C
ENST00000481849.6:n.3421A>C
ENST00000497377.6:n.3328A>C
ENST00000696558.1:c.1483A>C	ENSP00000512716.1:n.1483A>C
ENST00000696559.1:c.*325A>C	ENSP00000512717.1:n.*325A>C
ENST00000696560.1:c.*325A>C	ENSP00000512718.1:n.*325A>C
ENST00000696561.1:c.*325A>C	ENSP00000512719.1:n.*325A>C
ENST00000696562.1:c.*325A>C	ENSP00000512720.1:n.*325A>C
ENST00000412585.7:c.*325A>C MANE Select	ENSP00000399168.2:n.*325A>C
ENST00000412585.6:c.*325A>C	ENSP00000399168.2:n.*325A>C
ENST00000481849.5:n.649A>C
ENST00000497377.5:n.813A>C
NM_005514.6:c.*325A>C	NP_005505.2:n.*325A>C
XM_011514556.1:c.*325A>C	XP_011512858.1:n.*325A>C
XM_011514557.1:c.*325A>C	XP_011512859.1:n.*325A>C
XR_926175.1:n.1853A>C
NM_005514.7:c.*325A>C	NP_005505.2:n.*325A>C
NM_005514.8:c.*325A>C MANE Select	NP_005505.2:n.*325A>C