Canonical Allele Identifier: CA2677957755
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356825_31356826insTC , CM000668.2:g.31356825_31356826insTC GRCh38
NC_000006.11:g.31324602_31324603insTC , CM000668.1:g.31324602_31324603insTC GRCh37
NC_000006.10:g.31432581_31432582insTC NCBI36
NG_023187.1:g.5387_5388insGA

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1678_1679insGA
ENST00000481849.6:n.1678_1679insGA
ENST00000497377.6:n.1678_1679insGA
ENST00000640094.2:c.205_206insGA ENSP00000491275.2:p.Glu69GlyfsTer9
ENST00000696558.1:c.205_206insGA ENSP00000512716.1:p.Glu69GlyfsTer9
ENST00000696559.1:c.205_206insGA ENSP00000512717.1:p.Glu69GlyfsTer9
ENST00000696560.1:c.205_206insGA ENSP00000512718.1:p.Glu69GlyfsTer9
ENST00000696561.1:c.205_206insGA ENSP00000512719.1:p.Glu69GlyfsTer9
ENST00000696562.1:c.205_206insGA ENSP00000512720.1:p.Glu69GlyfsTer9
ENST00000412585.7:c.205_206insGA MANE Select ENSP00000399168.2:p.Glu69GlyfsTer9
ENST00000412585.6:c.205_206insGA ENSP00000399168.2:p.Glu69GlyfsTer9
ENST00000434333.1:c.238_239insGA ENSP00000405931.1:p.Glu80GlyfsTer9
ENST00000474381.1:n.80_81insGA
ENST00000498007.1:n.226_227insGA
ENST00000603274.1:n.179_180insTC
NM_005514.6:c.205_206insGA NP_005505.2:p.Glu69GlyfsTer9
XM_011514556.1:c.238_239insGA XP_011512858.1:p.Glu80GlyfsTer9
XM_011514557.1:c.205_206insGA XP_011512859.1:p.Glu69GlyfsTer9
XR_926175.1:n.215_216insGA
NM_005514.7:c.205_206insGA NP_005505.2:p.Glu69GlyfsTer9
NM_005514.8:c.205_206insGA MANE Select NP_005505.2:p.Glu69GlyfsTer9