Canonical Allele Identifier: CA2770503544

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354694_31354812del , CM000668.2:g.31354694_31354812del	GRCh38
NC_000006.11:g.31322471_31322589del , CM000668.1:g.31322471_31322589del	GRCh37
NC_000006.10:g.31430450_31430568del	NCBI36
NG_023187.1:g.7401_7519del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3060-147_3060-29del
ENST00000481849.6:n.2873_2991del
ENST00000497377.6:n.2780_2898del
ENST00000640094.2:c.896-147_896-29del	ENSP00000491275.2:n.896-147_896-29del
ENST00000696558.1:c.1082-147_1082-29del	ENSP00000512716.1:n.1082-147_1082-29del
ENST00000696559.1:c.1013-147_1013-29del	ENSP00000512717.1:n.1013-147_1013-29del
ENST00000696560.1:c.1013-147_1013-29del	ENSP00000512718.1:n.1013-147_1013-29del
ENST00000696561.1:c.1013-147_1013-29del	ENSP00000512719.1:n.1013-147_1013-29del
ENST00000696562.1:c.1013-147_1013-29del	ENSP00000512720.1:n.1013-147_1013-29del
ENST00000412585.7:c.1013-147_1013-29del MANE Select	ENSP00000399168.2:n.1013-147_1013-29del
ENST00000640094.1:c.89-147_89-29del	ENSP00000491275.1:n.89-147_89-29del
ENST00000412585.6:c.1013-147_1013-29del	ENSP00000399168.2:n.1013-147_1013-29del
ENST00000497377.5:n.265_383del
NM_005514.6:c.1013-147_1013-29del	NP_005505.2:n.1013-147_1013-29del
XM_011514556.1:c.1046-147_1046-29del	XP_011512858.1:n.1046-147_1046-29del
XM_011514557.1:c.896-147_896-29del	XP_011512859.1:n.896-147_896-29del
XR_926175.1:n.1452-147_1452-29del
NM_005514.7:c.1013-147_1013-29del	NP_005505.2:n.1013-147_1013-29del
NM_005514.8:c.1013-147_1013-29del MANE Select	NP_005505.2:n.1013-147_1013-29del