Canonical Allele Identifier: CA2770503560

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355029_31355030insTG , CM000668.2:g.31355029_31355030insTG	GRCh38
NC_000006.11:g.31322806_31322807insTG , CM000668.1:g.31322806_31322807insTG	GRCh37
NC_000006.10:g.31430785_31430786insTG	NCBI36
NG_023187.1:g.7183_7184insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3059+77_3059+78insCA
ENST00000481849.6:n.2655_2656insCA
ENST00000497377.6:n.2562_2563insCA
ENST00000640094.2:c.895+287_895+288insCA	ENSP00000491275.2:n.895+287_895+288insCA
ENST00000696558.1:c.1081+77_1081+78insCA	ENSP00000512716.1:n.1081+77_1081+78insCA
ENST00000696559.1:c.1012+77_1012+78insCA	ENSP00000512717.1:n.1012+77_1012+78insCA
ENST00000696560.1:c.1012+77_1012+78insCA	ENSP00000512718.1:n.1012+77_1012+78insCA
ENST00000696561.1:c.1012+77_1012+78insCA	ENSP00000512719.1:n.1012+77_1012+78insCA
ENST00000696562.1:c.1012+77_1012+78insCA	ENSP00000512720.1:n.1012+77_1012+78insCA
ENST00000412585.7:c.1012+77_1012+78insCA MANE Select	ENSP00000399168.2:n.1012+77_1012+78insCA
ENST00000640094.1:c.88+287_88+288insCA	ENSP00000491275.1:n.88+287_88+288insCA
ENST00000412585.6:c.1012+77_1012+78insCA	ENSP00000399168.2:n.1012+77_1012+78insCA
ENST00000497377.5:n.47_48insCA
NM_005514.6:c.1012+77_1012+78insCA	NP_005505.2:n.1012+77_1012+78insCA
XM_011514556.1:c.1045+77_1045+78insCA	XP_011512858.1:n.1045+77_1045+78insCA
XM_011514557.1:c.895+287_895+288insCA	XP_011512859.1:n.895+287_895+288insCA
XR_926175.1:n.1451+77_1451+78insCA
NM_005514.7:c.1012+77_1012+78insCA	NP_005505.2:n.1012+77_1012+78insCA
NM_005514.8:c.1012+77_1012+78insCA MANE Select	NP_005505.2:n.1012+77_1012+78insCA