Canonical Allele Identifier: CA2840254781

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354428_31354436del , CM000668.2:g.31354428_31354436del	GRCh38
NC_000006.11:g.31322205_31322213del , CM000668.1:g.31322205_31322213del	GRCh37
NC_000006.10:g.31430184_31430192del	NCBI36
NG_023187.1:g.7781_7789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+47_3140+55del
ENST00000481849.6:n.3100+47_3100+55del
ENST00000497377.6:n.3007+47_3007+55del
ENST00000696558.1:c.1162+47_1162+55del	ENSP00000512716.1:n.1162+47_1162+55del
ENST00000696559.1:c.*4+47_*4+55del	ENSP00000512717.1:n.*4+47_*4+55del
ENST00000696560.1:c.*4+47_*4+55del	ENSP00000512718.1:n.*4+47_*4+55del
ENST00000696561.1:c.*4+47_*4+55del	ENSP00000512719.1:n.*4+47_*4+55del
ENST00000696562.1:c.*4+47_*4+55del	ENSP00000512720.1:n.*4+47_*4+55del
ENST00000412585.7:c.*4+47_*4+55del MANE Select	ENSP00000399168.2:n.*4+47_*4+55del
ENST00000412585.6:c.*4+47_*4+55del	ENSP00000399168.2:n.*4+47_*4+55del
ENST00000481849.5:n.328+47_328+55del
ENST00000497377.5:n.492+47_492+55del
NM_005514.6:c.*4+47_*4+55del	NP_005505.2:n.*4+47_*4+55del
XM_011514556.1:c.*4+47_*4+55del	XP_011512858.1:n.*4+47_*4+55del
XM_011514557.1:c.*4+47_*4+55del	XP_011512859.1:n.*4+47_*4+55del
XR_926175.1:n.1532+47_1532+55del
NM_005514.7:c.*4+47_*4+55del	NP_005505.2:n.*4+47_*4+55del
NM_005514.8:c.*4+47_*4+55del MANE Select	NP_005505.2:n.*4+47_*4+55del