Canonical Allele Identifier: CA2677956411

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356096-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356096_31356097insTC , CM000668.2:g.31356096_31356097insTC	GRCh38
NC_000006.11:g.31323873_31323874insTC , CM000668.1:g.31323873_31323874insTC	GRCh37
NC_000006.10:g.31431852_31431853insTC	NCBI36
NG_023187.1:g.6116_6117insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2162_2163insGA
ENST00000481849.6:n.2092+70_2092+71insGA
ENST00000497377.6:n.2092+70_2092+71insGA
ENST00000640094.2:c.619+70_619+71insGA	ENSP00000491275.2:n.619+70_619+71insGA
ENST00000696558.1:c.619+70_619+71insGA	ENSP00000512716.1:n.619+70_619+71insGA
ENST00000696559.1:c.619+70_619+71insGA	ENSP00000512717.1:n.619+70_619+71insGA
ENST00000696560.1:c.619+70_619+71insGA	ENSP00000512718.1:n.619+70_619+71insGA
ENST00000696561.1:c.619+70_619+71insGA	ENSP00000512719.1:n.619+70_619+71insGA
ENST00000696562.1:c.619+70_619+71insGA	ENSP00000512720.1:n.619+70_619+71insGA
ENST00000412585.7:c.619+70_619+71insGA MANE Select	ENSP00000399168.2:n.619+70_619+71insGA
ENST00000412585.6:c.619+70_619+71insGA	ENSP00000399168.2:n.619+70_619+71insGA
ENST00000434333.1:c.652+70_652+71insGA	ENSP00000405931.1:n.652+70_652+71insGA
ENST00000474381.1:n.564_565insGA
ENST00000498007.1:n.885+70_885+71insGA
NM_005514.6:c.619+70_619+71insGA	NP_005505.2:n.619+70_619+71insGA
XM_011514556.1:c.652+70_652+71insGA	XP_011512858.1:n.652+70_652+71insGA
XM_011514557.1:c.619+70_619+71insGA	XP_011512859.1:n.619+70_619+71insGA
XR_926175.1:n.699_700insGA
NM_005514.7:c.619+70_619+71insGA	NP_005505.2:n.619+70_619+71insGA
NM_005514.8:c.619+70_619+71insGA MANE Select	NP_005505.2:n.619+70_619+71insGA