Canonical Allele Identifier: CA2770505951

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354220del , CM000668.2:g.31354220del	GRCh38
NC_000006.11:g.31321997del , CM000668.1:g.31321997del	GRCh37
NC_000006.10:g.31429976del	NCBI36
NG_023187.1:g.7994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3218del
ENST00000481849.6:n.3178del
ENST00000497377.6:n.3085del
ENST00000696558.1:c.1240del	ENSP00000512716.1:n.1240del
ENST00000696559.1:c.*82del	ENSP00000512717.1:n.*82del
ENST00000696560.1:c.*82del	ENSP00000512718.1:n.*82del
ENST00000696561.1:c.*82del	ENSP00000512719.1:n.*82del
ENST00000696562.1:c.*82del	ENSP00000512720.1:n.*82del
ENST00000412585.7:c.*82del MANE Select	ENSP00000399168.2:n.*82del
ENST00000412585.6:c.*82del	ENSP00000399168.2:n.*82del
ENST00000481849.5:n.406del
ENST00000497377.5:n.570del
NM_005514.6:c.*82del	NP_005505.2:n.*82del
XM_011514556.1:c.*82del	XP_011512858.1:n.*82del
XM_011514557.1:c.*82del	XP_011512859.1:n.*82del
XR_926175.1:n.1610del
NM_005514.7:c.*82del	NP_005505.2:n.*82del
NM_005514.8:c.*82del MANE Select	NP_005505.2:n.*82del