Canonical Allele Identifier: CA917712376

Gene: HLA-B

Linked Data

• dbSNP Id: rs1401245855

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357110_31357111delinsCT , CM000668.2:g.31357110_31357111delinsCT	GRCh38
NC_000006.11:g.31324887_31324888delinsCT , CM000668.1:g.31324887_31324888delinsCT	GRCh37
NC_000006.10:g.31432866_31432867delinsCT	NCBI36
NG_023187.1:g.5102_5103delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1521_1522delinsAG
ENST00000481849.6:n.1521_1522delinsAG
ENST00000497377.6:n.1521_1522delinsAG
ENST00000640094.2:c.48_49delinsAG	ENSP00000491275.2:p.Leu17Val
ENST00000696558.1:c.48_49delinsAG	ENSP00000512716.1:p.Leu17Val
ENST00000696559.1:c.48_49delinsAG	ENSP00000512717.1:p.Leu17Val
ENST00000696560.1:c.48_49delinsAG	ENSP00000512718.1:p.Leu17Val
ENST00000696561.1:c.48_49delinsAG	ENSP00000512719.1:p.Leu17Val
ENST00000696562.1:c.48_49delinsAG	ENSP00000512720.1:p.Leu17Val
ENST00000412585.7:c.48_49delinsAG MANE Select	ENSP00000399168.2:p.Leu17Val
ENST00000412585.6:c.48_49delinsAG	ENSP00000399168.2:p.Leu17Val
ENST00000434333.1:c.-48_-47delinsAG	ENSP00000405931.1:n.-48_-47delinsAG
ENST00000498007.1:n.69_70delinsAG
ENST00000603274.1:n.464_465delinsCT
NM_005514.6:c.48_49delinsAG	NP_005505.2:p.Leu17Val
XM_011514557.1:c.48_49delinsAG	XP_011512859.1:p.Leu17Val
XR_926175.1:n.58_59delinsAG
NM_005514.7:c.48_49delinsAG	NP_005505.2:p.Leu17Val
NM_005514.8:c.48_49delinsAG MANE Select	NP_005505.2:p.Leu17Val