Canonical Allele Identifier: CA1619118708
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355348_31355349delinsCT , CM000668.2:g.31355348_31355349delinsCT GRCh38
NC_000006.11:g.31323125_31323126delinsCT , CM000668.1:g.31323125_31323126delinsCT GRCh37
NC_000006.10:g.31431104_31431105delinsCT NCBI36
NG_023187.1:g.6864_6865delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2910_2911delinsAG
ENST00000481849.6:n.2336_2337delinsAG
ENST00000497377.6:n.2336_2337delinsAG
ENST00000640094.2:c.863_864delinsAG ENSP00000491275.2:p.Glu288=
ENST00000696558.1:c.932_933delinsAG ENSP00000512716.1:n.932_933delinsAG
ENST00000696559.1:c.863_864delinsAG ENSP00000512717.1:p.Glu288=
ENST00000696560.1:c.863_864delinsAG ENSP00000512718.1:p.Glu288=
ENST00000696561.1:c.863_864delinsAG ENSP00000512719.1:p.Glu288=
ENST00000696562.1:c.863_864delinsAG ENSP00000512720.1:p.Glu288=
ENST00000412585.7:c.863_864delinsAG MANE Select ENSP00000399168.2:p.Glu288=
ENST00000640094.1:c.56_57delinsAG ENSP00000491275.1:p.Glu19=
ENST00000412585.6:c.863_864delinsAG ENSP00000399168.2:p.Glu288=
ENST00000463574.1:n.454_455delinsAG
NM_005514.6:c.863_864delinsAG NP_005505.2:p.Glu288=
XM_011514556.1:c.896_897delinsAG XP_011512858.1:p.Glu299=
XM_011514557.1:c.863_864delinsAG XP_011512859.1:p.Glu288=
XR_926175.1:n.1302_1303delinsAG
NM_005514.7:c.863_864delinsAG NP_005505.2:p.Glu288=
NM_005514.8:c.863_864delinsAG MANE Select NP_005505.2:p.Glu288=