Canonical Allele Identifier: CA2770503566

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355110_31355111del , CM000668.2:g.31355110_31355111del	GRCh38
NC_000006.11:g.31322887_31322888del , CM000668.1:g.31322887_31322888del	GRCh37
NC_000006.10:g.31430866_31430867del	NCBI36
NG_023187.1:g.7102_7103del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3055_3056del
ENST00000481849.6:n.2574_2575del
ENST00000497377.6:n.2481_2482del
ENST00000640094.2:c.895+206_895+207del	ENSP00000491275.2:n.895+206_895+207del
ENST00000696558.1:c.1077_1078del	ENSP00000512716.1:n.1077_1078del
ENST00000696559.1:c.1008_1009del	ENSP00000512717.1:p.Ser337ArgfsTer20
ENST00000696560.1:c.1008_1009del	ENSP00000512718.1:p.Ser337ArgfsTer20
ENST00000696561.1:c.1008_1009del	ENSP00000512719.1:p.Ser337ArgfsTer20
ENST00000696562.1:c.1008_1009del	ENSP00000512720.1:p.Ser337ArgfsTer20
ENST00000412585.7:c.1008_1009del MANE Select	ENSP00000399168.2:p.Ser337ArgfsTer20
ENST00000640094.1:c.88+206_88+207del	ENSP00000491275.1:n.88+206_88+207del
ENST00000412585.6:c.1008_1009del	ENSP00000399168.2:p.Ser337ArgfsTer20
NM_005514.6:c.1008_1009del	NP_005505.2:p.Ser337ArgfsTer20
XM_011514556.1:c.1041_1042del	XP_011512858.1:p.Ser348ArgfsTer20
XM_011514557.1:c.895+206_895+207del	XP_011512859.1:n.895+206_895+207del
XR_926175.1:n.1447_1448del
NM_005514.7:c.1008_1009del	NP_005505.2:p.Ser337ArgfsTer20
NM_005514.8:c.1008_1009del MANE Select	NP_005505.2:p.Ser337ArgfsTer20