Canonical Allele Identifier: CA2770503453

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354399_31354400del , CM000668.2:g.31354399_31354400del	GRCh38
NC_000006.11:g.31322176_31322177del , CM000668.1:g.31322176_31322177del	GRCh37
NC_000006.10:g.31430155_31430156del	NCBI36
NG_023187.1:g.7815_7816del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+81_3140+82del
ENST00000481849.6:n.3100+81_3100+82del
ENST00000497377.6:n.3007+81_3007+82del
ENST00000696558.1:c.1162+81_1162+82del	ENSP00000512716.1:n.1162+81_1162+82del
ENST00000696559.1:c.*4+81_*4+82del	ENSP00000512717.1:n.*4+81_*4+82del
ENST00000696560.1:c.*4+81_*4+82del	ENSP00000512718.1:n.*4+81_*4+82del
ENST00000696561.1:c.*4+81_*4+82del	ENSP00000512719.1:n.*4+81_*4+82del
ENST00000696562.1:c.*4+81_*4+82del	ENSP00000512720.1:n.*4+81_*4+82del
ENST00000412585.7:c.*4+81_*4+82del MANE Select	ENSP00000399168.2:n.*4+81_*4+82del
ENST00000412585.6:c.*4+81_*4+82del	ENSP00000399168.2:n.*4+81_*4+82del
ENST00000481849.5:n.328+81_328+82del
ENST00000497377.5:n.492+81_492+82del
NM_005514.6:c.*4+81_*4+82del	NP_005505.2:n.*4+81_*4+82del
XM_011514556.1:c.*4+81_*4+82del	XP_011512858.1:n.*4+81_*4+82del
XM_011514557.1:c.*4+81_*4+82del	XP_011512859.1:n.*4+81_*4+82del
XR_926175.1:n.1532+81_1532+82del
NM_005514.7:c.*4+81_*4+82del	NP_005505.2:n.*4+81_*4+82del
NM_005514.8:c.*4+81_*4+82del MANE Select	NP_005505.2:n.*4+81_*4+82del