Canonical Allele Identifier: CA136832468

Gene: HLA-B

Linked Data

• dbSNP Id: rs41555514
• gnomAD v3: 6-31355162-T-G
• gnomAD v4: 6-31355162-T-G
• MyVariant Identifiers: chr6:g.31322939T>G (hg19) ; chr6:g.31355162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355162T>G , CM000668.2:g.31355162T>G	GRCh38
NC_000006.11:g.31322939T>G , CM000668.1:g.31322939T>G	GRCh37
NC_000006.10:g.31430918T>G	NCBI36
NG_023187.1:g.7051A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3004A>C
ENST00000481849.6:n.2523A>C
ENST00000497377.6:n.2430A>C
ENST00000640094.2:c.895+155A>C	ENSP00000491275.2:n.895+155A>C
ENST00000696558.1:c.1026A>C	ENSP00000512716.1:n.1026A>C
ENST00000696559.1:c.957A>C	ENSP00000512717.1:p.Ala319=
ENST00000696560.1:c.957A>C	ENSP00000512718.1:p.Ala319=
ENST00000696561.1:c.957A>C	ENSP00000512719.1:p.Ala319=
ENST00000696562.1:c.957A>C	ENSP00000512720.1:p.Ala319=
ENST00000412585.7:c.957A>C MANE Select	ENSP00000399168.2:p.Ala319=
ENST00000640094.1:c.88+155A>C	ENSP00000491275.1:n.88+155A>C
ENST00000412585.6:c.957A>C	ENSP00000399168.2:p.Ala319=
ENST00000463574.1:n.548A>C
NM_005514.6:c.957A>C	NP_005505.2:p.Ala319=
XM_011514556.1:c.990A>C	XP_011512858.1:p.Ala330=
XM_011514557.1:c.895+155A>C	XP_011512859.1:n.895+155A>C
XR_926175.1:n.1396A>C
NM_005514.7:c.957A>C	NP_005505.2:p.Ala319=
NM_005514.8:c.957A>C MANE Select	NP_005505.2:p.Ala319=