Canonical Allele Identifier: CA2770503690

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356190_31356191insACTGCCT , CM000668.2:g.31356190_31356191insACTGCCT	GRCh38
NC_000006.11:g.31323967_31323968insACTGCCT , CM000668.1:g.31323967_31323968insACTGCCT	GRCh37
NC_000006.10:g.31431946_31431947insACTGCCT	NCBI36
NG_023187.1:g.6022_6023insAGGCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2068_2069insAGGCAGT
ENST00000481849.6:n.2068_2069insAGGCAGT
ENST00000497377.6:n.2068_2069insAGGCAGT
ENST00000640094.2:c.595_596insAGGCAGT	ENSP00000491275.2:p.Gly199GlufsTer11
ENST00000696558.1:c.595_596insAGGCAGT	ENSP00000512716.1:p.Gly199GlufsTer11
ENST00000696559.1:c.595_596insAGGCAGT	ENSP00000512717.1:p.Gly199GlufsTer11
ENST00000696560.1:c.595_596insAGGCAGT	ENSP00000512718.1:p.Gly199GlufsTer11
ENST00000696561.1:c.595_596insAGGCAGT	ENSP00000512719.1:p.Gly199GlufsTer11
ENST00000696562.1:c.595_596insAGGCAGT	ENSP00000512720.1:p.Gly199GlufsTer11
ENST00000412585.7:c.595_596insAGGCAGT MANE Select	ENSP00000399168.2:p.Gly199GlufsTer11
ENST00000412585.6:c.595_596insAGGCAGT	ENSP00000399168.2:p.Gly199GlufsTer11
ENST00000434333.1:c.628_629insAGGCAGT	ENSP00000405931.1:p.Gly210GlufsTer11
ENST00000474381.1:n.470_471insAGGCAGT
ENST00000498007.1:n.861_862insAGGCAGT
NM_005514.6:c.595_596insAGGCAGT	NP_005505.2:p.Gly199GlufsTer11
XM_011514556.1:c.628_629insAGGCAGT	XP_011512858.1:p.Gly210GlufsTer11
XM_011514557.1:c.595_596insAGGCAGT	XP_011512859.1:p.Gly199GlufsTer11
XR_926175.1:n.605_606insAGGCAGT
NM_005514.7:c.595_596insAGGCAGT	NP_005505.2:p.Gly199GlufsTer11
NM_005514.8:c.595_596insAGGCAGT MANE Select	NP_005505.2:p.Gly199GlufsTer11