Canonical Allele Identifier: CA363308251

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31322427C>G (hg19) ; chr6:g.31354650C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354650C>G , CM000668.2:g.31354650C>G	GRCh38
NC_000006.11:g.31322427C>G , CM000668.1:g.31322427C>G	GRCh37
NC_000006.10:g.31430406C>G	NCBI36
NG_023187.1:g.7563G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3075G>C
ENST00000481849.6:n.3035G>C
ENST00000497377.6:n.2942G>C
ENST00000640094.2:c.911G>C	ENSP00000491275.2:p.Ser304Thr
ENST00000696558.1:c.1097G>C	ENSP00000512716.1:n.1097G>C
ENST00000696559.1:c.1028G>C	ENSP00000512717.1:p.Ser343Thr
ENST00000696560.1:c.1028G>C	ENSP00000512718.1:p.Ser343Thr
ENST00000696561.1:c.1028G>C	ENSP00000512719.1:p.Ser343Thr
ENST00000696562.1:c.1028G>C	ENSP00000512720.1:p.Ser343Thr
ENST00000412585.7:c.1028G>C MANE Select	ENSP00000399168.2:p.Ser343Thr
ENST00000640094.1:c.104G>C	ENSP00000491275.1:p.Ser35Thr
ENST00000412585.6:c.1028G>C	ENSP00000399168.2:p.Ser343Thr
ENST00000481849.5:n.157G>C
ENST00000497377.5:n.427G>C
NM_005514.6:c.1028G>C	NP_005505.2:p.Ser343Thr
XM_011514556.1:c.1061G>C	XP_011512858.1:p.Ser354Thr
XM_011514557.1:c.911G>C	XP_011512859.1:p.Ser304Thr
XR_926175.1:n.1467G>C
NM_005514.7:c.1028G>C	NP_005505.2:p.Ser343Thr
NM_005514.8:c.1028G>C MANE Select	NP_005505.2:p.Ser343Thr