Canonical Allele Identifier: CA3711835
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs766427608

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356827_31356830del , CM000668.2:g.31356827_31356830del GRCh38
NC_000006.11:g.31324604_31324607del , CM000668.1:g.31324604_31324607del GRCh37
NC_000006.10:g.31432583_31432586del NCBI36
NG_023187.1:g.5386_5389del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1677_1680del
ENST00000481849.6:n.1677_1680del
ENST00000497377.6:n.1677_1680del
ENST00000640094.2:c.204_207del ENSP00000491275.2:p.Glu69SerfsTer7
ENST00000696558.1:c.204_207del ENSP00000512716.1:p.Glu69SerfsTer7
ENST00000696559.1:c.204_207del ENSP00000512717.1:p.Glu69SerfsTer7
ENST00000696560.1:c.204_207del ENSP00000512718.1:p.Glu69SerfsTer7
ENST00000696561.1:c.204_207del ENSP00000512719.1:p.Glu69SerfsTer7
ENST00000696562.1:c.204_207del ENSP00000512720.1:p.Glu69SerfsTer7
ENST00000412585.7:c.204_207del MANE Select ENSP00000399168.2:p.Glu69SerfsTer7
ENST00000412585.6:c.204_207del ENSP00000399168.2:p.Glu69SerfsTer7
ENST00000434333.1:c.237_240del ENSP00000405931.1:p.Glu80SerfsTer7
ENST00000474381.1:n.79_82del
ENST00000498007.1:n.225_228del
ENST00000603274.1:n.181_184del
NM_005514.6:c.204_207del NP_005505.2:p.Glu69SerfsTer7
XM_011514556.1:c.237_240del XP_011512858.1:p.Glu80SerfsTer7
XM_011514557.1:c.204_207del XP_011512859.1:p.Glu69SerfsTer7
XR_926175.1:n.214_217del
NM_005514.7:c.204_207del NP_005505.2:p.Glu69SerfsTer7
NM_005514.8:c.204_207del MANE Select NP_005505.2:p.Glu69SerfsTer7