Canonical Allele Identifier: CA917712217

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554210404

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355134del , CM000668.2:g.31355134del	GRCh38
NC_000006.11:g.31322911del , CM000668.1:g.31322911del	GRCh37
NC_000006.10:g.31430890del	NCBI36
NG_023187.1:g.7079del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3032del
ENST00000481849.6:n.2551del
ENST00000497377.6:n.2458del
ENST00000640094.2:c.895+183del	ENSP00000491275.2:n.895+183del
ENST00000696558.1:c.1054del	ENSP00000512716.1:n.1054del
ENST00000696559.1:c.985del	ENSP00000512717.1:p.Ala329LeufsTer2
ENST00000696560.1:c.985del	ENSP00000512718.1:p.Ala329LeufsTer2
ENST00000696561.1:c.985del	ENSP00000512719.1:p.Ala329LeufsTer2
ENST00000696562.1:c.985del	ENSP00000512720.1:p.Ala329LeufsTer2
ENST00000412585.7:c.985del MANE Select	ENSP00000399168.2:p.Ala329LeufsTer2
ENST00000640094.1:c.88+183del	ENSP00000491275.1:n.88+183del
ENST00000412585.6:c.985del	ENSP00000399168.2:p.Ala329LeufsTer2
ENST00000463574.1:n.576del
NM_005514.6:c.985del	NP_005505.2:p.Ala329LeufsTer2
XM_011514556.1:c.1018del	XP_011512858.1:p.Ala340LeufsTer2
XM_011514557.1:c.895+183del	XP_011512859.1:n.895+183del
XR_926175.1:n.1424del
NM_005514.7:c.985del	NP_005505.2:p.Ala329LeufsTer2
NM_005514.8:c.985del MANE Select	NP_005505.2:p.Ala329LeufsTer2