Canonical Allele Identifier: CA2677956881

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356419-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356419_31356420insAC , CM000668.2:g.31356419_31356420insAC	GRCh38
NC_000006.11:g.31324196_31324197insAC , CM000668.1:g.31324196_31324197insAC	GRCh37
NC_000006.10:g.31432175_31432176insAC	NCBI36
NG_023187.1:g.5793_5794insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1839_1840insGT
ENST00000481849.6:n.1839_1840insGT
ENST00000497377.6:n.1839_1840insGT
ENST00000640094.2:c.366_367insGT	ENSP00000491275.2:p.Tyr123ValfsTer29
ENST00000696558.1:c.366_367insGT	ENSP00000512716.1:p.Tyr123ValfsTer29
ENST00000696559.1:c.366_367insGT	ENSP00000512717.1:p.Tyr123ValfsTer29
ENST00000696560.1:c.366_367insGT	ENSP00000512718.1:p.Tyr123ValfsTer29
ENST00000696561.1:c.366_367insGT	ENSP00000512719.1:p.Tyr123ValfsTer29
ENST00000696562.1:c.366_367insGT	ENSP00000512720.1:p.Tyr123ValfsTer29
ENST00000412585.7:c.366_367insGT MANE Select	ENSP00000399168.2:p.Tyr123ValfsTer29
ENST00000412585.6:c.366_367insGT	ENSP00000399168.2:p.Tyr123ValfsTer29
ENST00000434333.1:c.399_400insGT	ENSP00000405931.1:p.Tyr134ValfsTer29
ENST00000474381.1:n.241_242insGT
ENST00000498007.1:n.632_633insGT
NM_005514.6:c.366_367insGT	NP_005505.2:p.Tyr123ValfsTer29
XM_011514556.1:c.399_400insGT	XP_011512858.1:p.Tyr134ValfsTer29
XM_011514557.1:c.366_367insGT	XP_011512859.1:p.Tyr123ValfsTer29
XR_926175.1:n.376_377insGT
NM_005514.7:c.366_367insGT	NP_005505.2:p.Tyr123ValfsTer29
NM_005514.8:c.366_367insGT MANE Select	NP_005505.2:p.Tyr123ValfsTer29