Canonical Allele Identifier: CA2677956528

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356138-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356138_31356139insCA , CM000668.2:g.31356138_31356139insCA	GRCh38
NC_000006.11:g.31323915_31323916insCA , CM000668.1:g.31323915_31323916insCA	GRCh37
NC_000006.10:g.31431894_31431895insCA	NCBI36
NG_023187.1:g.6074_6075insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2120_2121insTG
ENST00000481849.6:n.2092+28_2092+29insTG
ENST00000497377.6:n.2092+28_2092+29insTG
ENST00000640094.2:c.619+28_619+29insTG	ENSP00000491275.2:n.619+28_619+29insTG
ENST00000696558.1:c.619+28_619+29insTG	ENSP00000512716.1:n.619+28_619+29insTG
ENST00000696559.1:c.619+28_619+29insTG	ENSP00000512717.1:n.619+28_619+29insTG
ENST00000696560.1:c.619+28_619+29insTG	ENSP00000512718.1:n.619+28_619+29insTG
ENST00000696561.1:c.619+28_619+29insTG	ENSP00000512719.1:n.619+28_619+29insTG
ENST00000696562.1:c.619+28_619+29insTG	ENSP00000512720.1:n.619+28_619+29insTG
ENST00000412585.7:c.619+28_619+29insTG MANE Select	ENSP00000399168.2:n.619+28_619+29insTG
ENST00000412585.6:c.619+28_619+29insTG	ENSP00000399168.2:n.619+28_619+29insTG
ENST00000434333.1:c.652+28_652+29insTG	ENSP00000405931.1:n.652+28_652+29insTG
ENST00000474381.1:n.522_523insTG
ENST00000498007.1:n.885+28_885+29insTG
NM_005514.6:c.619+28_619+29insTG	NP_005505.2:n.619+28_619+29insTG
XM_011514556.1:c.652+28_652+29insTG	XP_011512858.1:n.652+28_652+29insTG
XM_011514557.1:c.619+28_619+29insTG	XP_011512859.1:n.619+28_619+29insTG
XR_926175.1:n.657_658insTG
NM_005514.7:c.619+28_619+29insTG	NP_005505.2:n.619+28_619+29insTG
NM_005514.8:c.619+28_619+29insTG MANE Select	NP_005505.2:n.619+28_619+29insTG