Canonical Allele Identifier: CA2677957919

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357137-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357137_31357138insG , CM000668.2:g.31357137_31357138insG	GRCh38
NC_000006.11:g.31324914_31324915insG , CM000668.1:g.31324914_31324915insG	GRCh37
NC_000006.10:g.31432893_31432894insG	NCBI36
NG_023187.1:g.5075_5076insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1494_1495insC
ENST00000481849.6:n.1494_1495insC
ENST00000497377.6:n.1494_1495insC
ENST00000640094.2:c.21_22insC	ENSP00000491275.2:p.Thr8HisfsTer?
ENST00000696558.1:c.21_22insC	ENSP00000512716.1:p.Thr8HisfsTer?
ENST00000696559.1:c.21_22insC	ENSP00000512717.1:p.Thr8HisfsTer?
ENST00000696560.1:c.21_22insC	ENSP00000512718.1:p.Thr8HisfsTer?
ENST00000696561.1:c.21_22insC	ENSP00000512719.1:p.Thr8HisfsTer?
ENST00000696562.1:c.21_22insC	ENSP00000512720.1:p.Thr8HisfsTer?
ENST00000412585.7:c.21_22insC MANE Select	ENSP00000399168.2:p.Thr8HisfsTer?
ENST00000412585.6:c.21_22insC	ENSP00000399168.2:p.Thr8HisfsTer?
ENST00000434333.1:c.-75_-74insC	ENSP00000405931.1:n.-75_-74insC
ENST00000498007.1:n.42_43insC
ENST00000603274.1:n.491_492insG
NM_005514.6:c.21_22insC	NP_005505.2:p.Thr8HisfsTer?
XM_011514557.1:c.21_22insC	XP_011512859.1:p.Thr8HisfsTer?
XR_926175.1:n.31_32insC
NM_005514.7:c.21_22insC	NP_005505.2:p.Thr8HisfsTer?
NM_005514.8:c.21_22insC MANE Select	NP_005505.2:p.Thr8HisfsTer?