Canonical Allele Identifier: CA917712253

Gene: HLA-B

Linked Data

• dbSNP Id: rs1562167157

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356194_31356202del , CM000668.2:g.31356194_31356202del	GRCh38
NC_000006.11:g.31323971_31323979del , CM000668.1:g.31323971_31323979del	GRCh37
NC_000006.10:g.31431950_31431958del	NCBI36
NG_023187.1:g.6013_6021del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2059_2067del
ENST00000481849.6:n.2059_2067del
ENST00000497377.6:n.2059_2067del
ENST00000640094.2:c.586_594del	ENSP00000491275.2:p.Leu196_Asn198del
ENST00000696558.1:c.586_594del	ENSP00000512716.1:p.Leu196_Asn198del
ENST00000696559.1:c.586_594del	ENSP00000512717.1:p.Leu196_Asn198del
ENST00000696560.1:c.586_594del	ENSP00000512718.1:p.Leu196_Asn198del
ENST00000696561.1:c.586_594del	ENSP00000512719.1:p.Leu196_Asn198del
ENST00000696562.1:c.586_594del	ENSP00000512720.1:p.Leu196_Asn198del
ENST00000412585.7:c.586_594del MANE Select	ENSP00000399168.2:p.Leu196_Asn198del
ENST00000412585.6:c.586_594del	ENSP00000399168.2:p.Leu196_Asn198del
ENST00000434333.1:c.619_627del	ENSP00000405931.1:p.Leu207_Asn209del
ENST00000474381.1:n.461_469del
ENST00000498007.1:n.852_860del
NM_005514.6:c.586_594del	NP_005505.2:p.Leu196_Asn198del
XM_011514556.1:c.619_627del	XP_011512858.1:p.Leu207_Asn209del
XM_011514557.1:c.586_594del	XP_011512859.1:p.Leu196_Asn198del
XR_926175.1:n.596_604del
NM_005514.7:c.586_594del	NP_005505.2:p.Leu196_Asn198del
NM_005514.8:c.586_594del MANE Select	NP_005505.2:p.Leu196_Asn198del