Canonical Allele Identifier: CA2677956950

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356433-G-GCCAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356433_31356434insCCAAT , CM000668.2:g.31356433_31356434insCCAAT	GRCh38
NC_000006.11:g.31324210_31324211insCCAAT , CM000668.1:g.31324210_31324211insCCAAT	GRCh37
NC_000006.10:g.31432189_31432190insCCAAT	NCBI36
NG_023187.1:g.5779_5780insATTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1825_1826insATTGG
ENST00000481849.6:n.1825_1826insATTGG
ENST00000497377.6:n.1825_1826insATTGG
ENST00000640094.2:c.352_353insATTGG	ENSP00000491275.2:p.Thr118AsnfsTer?
ENST00000696558.1:c.352_353insATTGG	ENSP00000512716.1:p.Thr118AsnfsTer?
ENST00000696559.1:c.352_353insATTGG	ENSP00000512717.1:p.Thr118AsnfsTer?
ENST00000696560.1:c.352_353insATTGG	ENSP00000512718.1:p.Thr118AsnfsTer?
ENST00000696561.1:c.352_353insATTGG	ENSP00000512719.1:p.Thr118AsnfsTer?
ENST00000696562.1:c.352_353insATTGG	ENSP00000512720.1:p.Thr118AsnfsTer?
ENST00000412585.7:c.352_353insATTGG MANE Select	ENSP00000399168.2:p.Thr118AsnfsTer?
ENST00000412585.6:c.352_353insATTGG	ENSP00000399168.2:p.Thr118AsnfsTer?
ENST00000434333.1:c.385_386insATTGG	ENSP00000405931.1:p.Thr129AsnfsTer?
ENST00000474381.1:n.227_228insATTGG
ENST00000498007.1:n.618_619insATTGG
NM_005514.6:c.352_353insATTGG	NP_005505.2:p.Thr118AsnfsTer?
XM_011514556.1:c.385_386insATTGG	XP_011512858.1:p.Thr129AsnfsTer?
XM_011514557.1:c.352_353insATTGG	XP_011512859.1:p.Thr118AsnfsTer?
XR_926175.1:n.362_363insATTGG
NM_005514.7:c.352_353insATTGG	NP_005505.2:p.Thr118AsnfsTer?
NM_005514.8:c.352_353insATTGG MANE Select	NP_005505.2:p.Thr118AsnfsTer?