Canonical Allele Identifier: CA2770505958

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354327_31354340del , CM000668.2:g.31354327_31354340del	GRCh38
NC_000006.11:g.31322104_31322117del , CM000668.1:g.31322104_31322117del	GRCh37
NC_000006.10:g.31430083_31430096del	NCBI36
NG_023187.1:g.7873_7886del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3141-44_3141-31del
ENST00000481849.6:n.3101-44_3101-31del
ENST00000497377.6:n.3008-44_3008-31del
ENST00000696558.1:c.1163-44_1163-31del	ENSP00000512716.1:n.1163-44_1163-31del
ENST00000696559.1:c.*5-44_*5-31del	ENSP00000512717.1:n.*5-44_*5-31del
ENST00000696560.1:c.*5-44_*5-31del	ENSP00000512718.1:n.*5-44_*5-31del
ENST00000696561.1:c.*5-44_*5-31del	ENSP00000512719.1:n.*5-44_*5-31del
ENST00000696562.1:c.*5-44_*5-31del	ENSP00000512720.1:n.*5-44_*5-31del
ENST00000412585.7:c.*5-44_*5-31del MANE Select	ENSP00000399168.2:n.*5-44_*5-31del
ENST00000412585.6:c.*5-44_*5-31del	ENSP00000399168.2:n.*5-44_*5-31del
ENST00000481849.5:n.329-44_329-31del
ENST00000497377.5:n.493-44_493-31del
NM_005514.6:c.*5-44_*5-31del	NP_005505.2:n.*5-44_*5-31del
XM_011514556.1:c.*5-44_*5-31del	XP_011512858.1:n.*5-44_*5-31del
XM_011514557.1:c.*5-44_*5-31del	XP_011512859.1:n.*5-44_*5-31del
XR_926175.1:n.1533-44_1533-31del
NM_005514.7:c.*5-44_*5-31del	NP_005505.2:n.*5-44_*5-31del
NM_005514.8:c.*5-44_*5-31del MANE Select	NP_005505.2:n.*5-44_*5-31del