Canonical Allele Identifier: CA2770503559

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355027_31355028del , CM000668.2:g.31355027_31355028del	GRCh38
NC_000006.11:g.31322804_31322805del , CM000668.1:g.31322804_31322805del	GRCh37
NC_000006.10:g.31430783_31430784del	NCBI36
NG_023187.1:g.7185_7186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+79_3059+80del
ENST00000481849.6:n.2657_2658del
ENST00000497377.6:n.2564_2565del
ENST00000640094.2:c.895+289_895+290del	ENSP00000491275.2:n.895+289_895+290del
ENST00000696558.1:c.1081+79_1081+80del	ENSP00000512716.1:n.1081+79_1081+80del
ENST00000696559.1:c.1012+79_1012+80del	ENSP00000512717.1:n.1012+79_1012+80del
ENST00000696560.1:c.1012+79_1012+80del	ENSP00000512718.1:n.1012+79_1012+80del
ENST00000696561.1:c.1012+79_1012+80del	ENSP00000512719.1:n.1012+79_1012+80del
ENST00000696562.1:c.1012+79_1012+80del	ENSP00000512720.1:n.1012+79_1012+80del
ENST00000412585.7:c.1012+79_1012+80del MANE Select	ENSP00000399168.2:n.1012+79_1012+80del
ENST00000640094.1:c.88+289_88+290del	ENSP00000491275.1:n.88+289_88+290del
ENST00000412585.6:c.1012+79_1012+80del	ENSP00000399168.2:n.1012+79_1012+80del
ENST00000497377.5:n.49_50del
NM_005514.6:c.1012+79_1012+80del	NP_005505.2:n.1012+79_1012+80del
XM_011514556.1:c.1045+79_1045+80del	XP_011512858.1:n.1045+79_1045+80del
XM_011514557.1:c.895+289_895+290del	XP_011512859.1:n.895+289_895+290del
XR_926175.1:n.1451+79_1451+80del
NM_005514.7:c.1012+79_1012+80del	NP_005505.2:n.1012+79_1012+80del
NM_005514.8:c.1012+79_1012+80del MANE Select	NP_005505.2:n.1012+79_1012+80del