Canonical Allele Identifier: CA363310272

Gene: HLA-B

Linked Data

• COSMIC: COSM4606010
• MyVariant Identifiers: chr6:g.31323141C>T (hg19) ; chr6:g.31355364C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355364C>T , CM000668.2:g.31355364C>T	GRCh38
NC_000006.11:g.31323141C>T , CM000668.1:g.31323141C>T	GRCh37
NC_000006.10:g.31431120C>T	NCBI36
NG_023187.1:g.6849G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2895G>A
ENST00000481849.6:n.2321G>A
ENST00000497377.6:n.2321G>A
ENST00000640094.2:c.848G>A	ENSP00000491275.2:p.Cys283Tyr
ENST00000696558.1:c.917G>A	ENSP00000512716.1:n.917G>A
ENST00000696559.1:c.848G>A	ENSP00000512717.1:p.Cys283Tyr
ENST00000696560.1:c.848G>A	ENSP00000512718.1:p.Cys283Tyr
ENST00000696561.1:c.848G>A	ENSP00000512719.1:p.Cys283Tyr
ENST00000696562.1:c.848G>A	ENSP00000512720.1:p.Cys283Tyr
ENST00000412585.7:c.848G>A MANE Select	ENSP00000399168.2:p.Cys283Tyr
ENST00000640094.1:c.41G>A	ENSP00000491275.1:p.Cys14Tyr
ENST00000412585.6:c.848G>A	ENSP00000399168.2:p.Cys283Tyr
ENST00000463574.1:n.439G>A
NM_005514.6:c.848G>A	NP_005505.2:p.Cys283Tyr
XM_011514556.1:c.881G>A	XP_011512858.1:p.Cys294Tyr
XM_011514557.1:c.848G>A	XP_011512859.1:p.Cys283Tyr
XR_926175.1:n.1287G>A
NM_005514.7:c.848G>A	NP_005505.2:p.Cys283Tyr
NM_005514.8:c.848G>A MANE Select	NP_005505.2:p.Cys283Tyr