Canonical Allele Identifier: CA2677957808

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356931-T-TATTTCCACACCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356931_31356932insATTTCCACACCTCC , CM000668.2:g.31356931_31356932insATTTCCACACCTCC	GRCh38
NC_000006.11:g.31324708_31324709insATTTCCACACCTCC , CM000668.1:g.31324708_31324709insATTTCCACACCTCC	GRCh37
NC_000006.10:g.31432687_31432688insATTTCCACACCTCC	NCBI36
NG_023187.1:g.5281_5282insGGAGGTGTGGAAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1572_1573insGGAGGTGTGGAAAT
ENST00000481849.6:n.1572_1573insGGAGGTGTGGAAAT
ENST00000497377.6:n.1572_1573insGGAGGTGTGGAAAT
ENST00000640094.2:c.99_100insGGAGGTGTGGAAAT	ENSP00000491275.2:p.Thr34GlyfsTer30
ENST00000696558.1:c.99_100insGGAGGTGTGGAAAT	ENSP00000512716.1:p.Thr34GlyfsTer30
ENST00000696559.1:c.99_100insGGAGGTGTGGAAAT	ENSP00000512717.1:p.Thr34GlyfsTer30
ENST00000696560.1:c.99_100insGGAGGTGTGGAAAT	ENSP00000512718.1:p.Thr34GlyfsTer30
ENST00000696561.1:c.99_100insGGAGGTGTGGAAAT	ENSP00000512719.1:p.Thr34GlyfsTer30
ENST00000696562.1:c.99_100insGGAGGTGTGGAAAT	ENSP00000512720.1:p.Thr34GlyfsTer30
ENST00000412585.7:c.99_100insGGAGGTGTGGAAAT MANE Select	ENSP00000399168.2:p.Thr34GlyfsTer30
ENST00000412585.6:c.99_100insGGAGGTGTGGAAAT	ENSP00000399168.2:p.Thr34GlyfsTer30
ENST00000434333.1:c.132_133insGGAGGTGTGGAAAT	ENSP00000405931.1:p.Thr45GlyfsTer30
ENST00000498007.1:n.120_121insGGAGGTGTGGAAAT
ENST00000603274.1:n.285_286insATTTCCACACCTCC
NM_005514.6:c.99_100insGGAGGTGTGGAAAT	NP_005505.2:p.Thr34GlyfsTer30
XM_011514556.1:c.132_133insGGAGGTGTGGAAAT	XP_011512858.1:p.Thr45GlyfsTer30
XM_011514557.1:c.99_100insGGAGGTGTGGAAAT	XP_011512859.1:p.Thr34GlyfsTer30
XR_926175.1:n.109_110insGGAGGTGTGGAAAT
NM_005514.7:c.99_100insGGAGGTGTGGAAAT	NP_005505.2:p.Thr34GlyfsTer30
NM_005514.8:c.99_100insGGAGGTGTGGAAAT MANE Select	NP_005505.2:p.Thr34GlyfsTer30