Canonical Allele Identifier: CA136832416

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554210405

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355133del , CM000668.2:g.31355133del	GRCh38
NC_000006.11:g.31322910del , CM000668.1:g.31322910del	GRCh37
NC_000006.10:g.31430889del	NCBI36
NG_023187.1:g.7080del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3033del
ENST00000481849.6:n.2552del
ENST00000497377.6:n.2459del
ENST00000640094.2:c.895+184del	ENSP00000491275.2:n.895+184del
ENST00000696558.1:c.1055del	ENSP00000512716.1:n.1055del
ENST00000696559.1:c.986del	ENSP00000512717.1:p.Ala329ValfsTer2
ENST00000696560.1:c.986del	ENSP00000512718.1:p.Ala329ValfsTer2
ENST00000696561.1:c.986del	ENSP00000512719.1:p.Ala329ValfsTer2
ENST00000696562.1:c.986del	ENSP00000512720.1:p.Ala329ValfsTer2
ENST00000412585.7:c.986del MANE Select	ENSP00000399168.2:p.Ala329ValfsTer2
ENST00000640094.1:c.88+184del	ENSP00000491275.1:n.88+184del
ENST00000412585.6:c.986del	ENSP00000399168.2:p.Ala329ValfsTer2
ENST00000463574.1:n.577del
NM_005514.6:c.986del	NP_005505.2:p.Ala329ValfsTer2
XM_011514556.1:c.1019del	XP_011512858.1:p.Ala340ValfsTer2
XM_011514557.1:c.895+184del	XP_011512859.1:n.895+184del
XR_926175.1:n.1425del
NM_005514.7:c.986del	NP_005505.2:p.Ala329ValfsTer2
NM_005514.8:c.986del MANE Select	NP_005505.2:p.Ala329ValfsTer2