Canonical Allele Identifier: CA2677956889

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356421-A-ACC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356421_31356422insCC , CM000668.2:g.31356421_31356422insCC	GRCh38
NC_000006.11:g.31324198_31324199insCC , CM000668.1:g.31324198_31324199insCC	GRCh37
NC_000006.10:g.31432177_31432178insCC	NCBI36
NG_023187.1:g.5791_5792insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1837_1838insGG
ENST00000481849.6:n.1837_1838insGG
ENST00000497377.6:n.1837_1838insGG
ENST00000640094.2:c.364_365insGG	ENSP00000491275.2:p.Met122ArgfsTer30
ENST00000696558.1:c.364_365insGG	ENSP00000512716.1:p.Met122ArgfsTer30
ENST00000696559.1:c.364_365insGG	ENSP00000512717.1:p.Met122ArgfsTer30
ENST00000696560.1:c.364_365insGG	ENSP00000512718.1:p.Met122ArgfsTer30
ENST00000696561.1:c.364_365insGG	ENSP00000512719.1:p.Met122ArgfsTer30
ENST00000696562.1:c.364_365insGG	ENSP00000512720.1:p.Met122ArgfsTer30
ENST00000412585.7:c.364_365insGG MANE Select	ENSP00000399168.2:p.Met122ArgfsTer30
ENST00000412585.6:c.364_365insGG	ENSP00000399168.2:p.Met122ArgfsTer30
ENST00000434333.1:c.397_398insGG	ENSP00000405931.1:p.Met133ArgfsTer30
ENST00000474381.1:n.239_240insGG
ENST00000498007.1:n.630_631insGG
NM_005514.6:c.364_365insGG	NP_005505.2:p.Met122ArgfsTer30
XM_011514556.1:c.397_398insGG	XP_011512858.1:p.Met133ArgfsTer30
XM_011514557.1:c.364_365insGG	XP_011512859.1:p.Met122ArgfsTer30
XR_926175.1:n.374_375insGG
NM_005514.7:c.364_365insGG	NP_005505.2:p.Met122ArgfsTer30
NM_005514.8:c.364_365insGG MANE Select	NP_005505.2:p.Met122ArgfsTer30