Canonical Allele Identifier: CA136836051

Gene: HLA-B

Linked Data

• dbSNP Id: rs1554211632

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356417_31356431delinsAGACATCCTCTGGAT , CM000668.2:g.31356417_31356431delinsAGACATCCTCTGGAT	GRCh38
NC_000006.11:g.31324194_31324208delinsAGACATCCTCTGGAT , CM000668.1:g.31324194_31324208delinsAGACATCCTCTGGAT	GRCh37
NC_000006.10:g.31432173_31432187delinsAGACATCCTCTGGAT	NCBI36
NG_023187.1:g.5782_5796delinsATCCAGAGGATGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1828_1842delinsATCCAGAGGATGTCT
ENST00000481849.6:n.1828_1842delinsATCCAGAGGATGTCT
ENST00000497377.6:n.1828_1842delinsATCCAGAGGATGTCT
ENST00000640094.2:c.355_369delinsATCCAGAGGATGTCT	ENSP00000491275.2:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000696558.1:c.355_369delinsATCCAGAGGATGTCT	ENSP00000512716.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000696559.1:c.355_369delinsATCCAGAGGATGTCT	ENSP00000512717.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000696560.1:c.355_369delinsATCCAGAGGATGTCT	ENSP00000512718.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000696561.1:c.355_369delinsATCCAGAGGATGTCT	ENSP00000512719.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000696562.1:c.355_369delinsATCCAGAGGATGTCT	ENSP00000512720.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000412585.7:c.355_369delinsATCCAGAGGATGTCT MANE Select	ENSP00000399168.2:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000412585.6:c.355_369delinsATCCAGAGGATGTCT	ENSP00000399168.2:p.Leu119_Tyr123delinsIleGlnArgMetSer
ENST00000434333.1:c.388_402delinsATCCAGAGGATGTCT	ENSP00000405931.1:p.Leu130_Tyr134delinsIleGlnArgMetSer
ENST00000474381.1:n.230_244delinsATCCAGAGGATGTCT
ENST00000498007.1:n.621_635delinsATCCAGAGGATGTCT
NM_005514.6:c.355_369delinsATCCAGAGGATGTCT	NP_005505.2:p.Leu119_Tyr123delinsIleGlnArgMetSer
XM_011514556.1:c.388_402delinsATCCAGAGGATGTCT	XP_011512858.1:p.Leu130_Tyr134delinsIleGlnArgMetSer
XM_011514557.1:c.355_369delinsATCCAGAGGATGTCT	XP_011512859.1:p.Leu119_Tyr123delinsIleGlnArgMetSer
XR_926175.1:n.365_379delinsATCCAGAGGATGTCT
NM_005514.7:c.355_369delinsATCCAGAGGATGTCT	NP_005505.2:p.Leu119_Tyr123delinsIleGlnArgMetSer
NM_005514.8:c.355_369delinsATCCAGAGGATGTCT MANE Select	NP_005505.2:p.Leu119_Tyr123delinsIleGlnArgMetSer