Canonical Allele Identifier: CA2770503558

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355018_31355027del , CM000668.2:g.31355018_31355027del	GRCh38
NC_000006.11:g.31322795_31322804del , CM000668.1:g.31322795_31322804del	GRCh37
NC_000006.10:g.31430774_31430783del	NCBI36
NG_023187.1:g.7186_7195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+80_3059+89del
ENST00000481849.6:n.2658_2667del
ENST00000497377.6:n.2565_2574del
ENST00000640094.2:c.895+290_895+299del	ENSP00000491275.2:n.895+290_895+299del
ENST00000696558.1:c.1081+80_1081+89del	ENSP00000512716.1:n.1081+80_1081+89del
ENST00000696559.1:c.1012+80_1012+89del	ENSP00000512717.1:n.1012+80_1012+89del
ENST00000696560.1:c.1012+80_1012+89del	ENSP00000512718.1:n.1012+80_1012+89del
ENST00000696561.1:c.1012+80_1012+89del	ENSP00000512719.1:n.1012+80_1012+89del
ENST00000696562.1:c.1012+80_1012+89del	ENSP00000512720.1:n.1012+80_1012+89del
ENST00000412585.7:c.1012+80_1012+89del MANE Select	ENSP00000399168.2:n.1012+80_1012+89del
ENST00000640094.1:c.88+290_88+299del	ENSP00000491275.1:n.88+290_88+299del
ENST00000412585.6:c.1012+80_1012+89del	ENSP00000399168.2:n.1012+80_1012+89del
ENST00000497377.5:n.50_59del
NM_005514.6:c.1012+80_1012+89del	NP_005505.2:n.1012+80_1012+89del
XM_011514556.1:c.1045+80_1045+89del	XP_011512858.1:n.1045+80_1045+89del
XM_011514557.1:c.895+290_895+299del	XP_011512859.1:n.895+290_895+299del
XR_926175.1:n.1451+80_1451+89del
NM_005514.7:c.1012+80_1012+89del	NP_005505.2:n.1012+80_1012+89del
NM_005514.8:c.1012+80_1012+89del MANE Select	NP_005505.2:n.1012+80_1012+89del