Canonical Allele Identifier: CA1087466539

Gene: HLA-B

Linked Data

• dbSNP Id: rs2113740306
• gnomAD v3: 6-31355899-A-AG
• gnomAD v4: 6-31355899-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355899_31355900insG , CM000668.2:g.31355899_31355900insG	GRCh38
NC_000006.11:g.31323676_31323677insG , CM000668.1:g.31323676_31323677insG	GRCh37
NC_000006.10:g.31431655_31431656insG	NCBI36
NG_023187.1:g.6313_6314insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2359_2360insC
ENST00000481849.6:n.2092+267_2092+268insC
ENST00000497377.6:n.2092+267_2092+268insC
ENST00000640094.2:c.619+267_619+268insC	ENSP00000491275.2:n.619+267_619+268insC
ENST00000696558.1:c.620-94_620-93insC	ENSP00000512716.1:n.620-94_620-93insC
ENST00000696559.1:c.619+267_619+268insC	ENSP00000512717.1:n.619+267_619+268insC
ENST00000696560.1:c.619+267_619+268insC	ENSP00000512718.1:n.619+267_619+268insC
ENST00000696561.1:c.619+267_619+268insC	ENSP00000512719.1:n.619+267_619+268insC
ENST00000696562.1:c.619+267_619+268insC	ENSP00000512720.1:n.619+267_619+268insC
ENST00000412585.7:c.619+267_619+268insC MANE Select	ENSP00000399168.2:n.619+267_619+268insC
ENST00000412585.6:c.619+267_619+268insC	ENSP00000399168.2:n.619+267_619+268insC
ENST00000434333.1:c.652+267_652+268insC	ENSP00000405931.1:n.652+267_652+268insC
ENST00000474381.1:n.761_762insC
ENST00000498007.1:n.885+267_885+268insC
NM_005514.6:c.619+267_619+268insC	NP_005505.2:n.619+267_619+268insC
XM_011514556.1:c.652+267_652+268insC	XP_011512858.1:n.652+267_652+268insC
XM_011514557.1:c.619+267_619+268insC	XP_011512859.1:n.619+267_619+268insC
XR_926175.1:n.896_897insC
NM_005514.7:c.619+267_619+268insC	NP_005505.2:n.619+267_619+268insC
NM_005514.8:c.619+267_619+268insC MANE Select	NP_005505.2:n.619+267_619+268insC