Canonical Allele Identifier: CA2677956410

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356096-T-TCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356097_31356098insGC , CM000668.2:g.31356097_31356098insGC	GRCh38
NC_000006.11:g.31323874_31323875insGC , CM000668.1:g.31323874_31323875insGC	GRCh37
NC_000006.10:g.31431853_31431854insGC	NCBI36
NG_023187.1:g.6116_6117insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2162_2163insCG
ENST00000481849.6:n.2092+70_2092+71insCG
ENST00000497377.6:n.2092+70_2092+71insCG
ENST00000640094.2:c.619+70_619+71insCG	ENSP00000491275.2:n.619+70_619+71insCG
ENST00000696558.1:c.619+70_619+71insCG	ENSP00000512716.1:n.619+70_619+71insCG
ENST00000696559.1:c.619+70_619+71insCG	ENSP00000512717.1:n.619+70_619+71insCG
ENST00000696560.1:c.619+70_619+71insCG	ENSP00000512718.1:n.619+70_619+71insCG
ENST00000696561.1:c.619+70_619+71insCG	ENSP00000512719.1:n.619+70_619+71insCG
ENST00000696562.1:c.619+70_619+71insCG	ENSP00000512720.1:n.619+70_619+71insCG
ENST00000412585.7:c.619+70_619+71insCG MANE Select	ENSP00000399168.2:n.619+70_619+71insCG
ENST00000412585.6:c.619+70_619+71insCG	ENSP00000399168.2:n.619+70_619+71insCG
ENST00000434333.1:c.652+70_652+71insCG	ENSP00000405931.1:n.652+70_652+71insCG
ENST00000474381.1:n.564_565insCG
ENST00000498007.1:n.885+70_885+71insCG
NM_005514.6:c.619+70_619+71insCG	NP_005505.2:n.619+70_619+71insCG
XM_011514556.1:c.652+70_652+71insCG	XP_011512858.1:n.652+70_652+71insCG
XM_011514557.1:c.619+70_619+71insCG	XP_011512859.1:n.619+70_619+71insCG
XR_926175.1:n.699_700insCG
NM_005514.7:c.619+70_619+71insCG	NP_005505.2:n.619+70_619+71insCG
NM_005514.8:c.619+70_619+71insCG MANE Select	NP_005505.2:n.619+70_619+71insCG