Canonical Allele Identifier: CA645561027
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356729_31356730delinsTC , CM000668.2:g.31356729_31356730delinsTC GRCh38
NC_000006.11:g.31324506_31324507delinsTC , CM000668.1:g.31324506_31324507delinsTC GRCh37
NC_000006.10:g.31432485_31432486delinsTC NCBI36
NG_023187.1:g.5483_5484delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1774_1775delinsGA
ENST00000481849.6:n.1774_1775delinsGA
ENST00000497377.6:n.1774_1775delinsGA
ENST00000640094.2:c.301_302delinsGA ENSP00000491275.2:p.Ser101Asp
ENST00000696558.1:c.301_302delinsGA ENSP00000512716.1:p.Ser101Asp
ENST00000696559.1:c.301_302delinsGA ENSP00000512717.1:p.Ser101Asp
ENST00000696560.1:c.301_302delinsGA ENSP00000512718.1:p.Ser101Asp
ENST00000696561.1:c.301_302delinsGA ENSP00000512719.1:p.Ser101Asp
ENST00000696562.1:c.301_302delinsGA ENSP00000512720.1:p.Ser101Asp
ENST00000412585.7:c.301_302delinsGA MANE Select ENSP00000399168.2:p.Ser101Asp
ENST00000412585.6:c.301_302delinsGA ENSP00000399168.2:p.Ser101Asp
ENST00000434333.1:c.334_335delinsGA ENSP00000405931.1:p.Ser112Asp
ENST00000474381.1:n.176_177delinsGA
ENST00000498007.1:n.322_323delinsGA
ENST00000603274.1:n.83_84delinsTC
NM_005514.6:c.301_302delinsGA NP_005505.2:p.Ser101Asp
XM_011514556.1:c.334_335delinsGA XP_011512858.1:p.Ser112Asp
XM_011514557.1:c.301_302delinsGA XP_011512859.1:p.Ser101Asp
XR_926175.1:n.311_312delinsGA
NM_005514.7:c.301_302delinsGA NP_005505.2:p.Ser101Asp
NM_005514.8:c.301_302delinsGA MANE Select NP_005505.2:p.Ser101Asp