Canonical Allele Identifier: CA1671914686
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149378081G= , CM000668.2:g.149378081G= GRCh38
NC_000006.11:g.149699217G= , CM000668.1:g.149699217G= GRCh37
NC_000006.10:g.149740910G= NCBI36
NG_021386.1:g.64782G=
NG_021386.2:g.165158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.581G=
ENST00000703213.1:c.166G= ENSP00000515239.1:p.Gly56=
ENST00000636456.1:c.-96-591G= ENSP00000490379.1:n.-96-591G=
ENST00000637181.2:c.166G= MANE Select ENSP00000490618.1:p.Gly56=
ENST00000367456.5:c.166G= ENSP00000356426.1:p.Gly56=
ENST00000470466.5:c.166G= ENSP00000432709.1:p.Gly56=
ENST00000538427.5:c.166G= ENSP00000445752.1:p.Gly56=
ENST00000606202.1:c.-57G= ENSP00000476139.1:n.-57G=
NM_001292034.2:c.166G= NP_001278963.1:p.Gly56=
NM_001292035.2:c.70G= NP_001278964.1:p.Gly24=
NM_015093.5:c.166G= NP_055908.1:p.Gly56=
XM_006715403.2:c.166G= XP_006715466.1:p.Gly56=
XM_011535633.1:c.166G= XP_011533935.1:p.Gly56=
XM_011535634.1:c.166G= XP_011533936.1:p.Gly56=
XM_011535633.2:c.166G= XP_011533935.1:p.Gly56=
XM_017010591.1:c.166G= XP_016866080.1:p.Gly56=
XM_017010592.2:c.166G= XP_016866081.1:p.Gly56=
NM_001292034.3:c.166G= MANE Select NP_001278963.1:p.Gly56=
NM_001292035.3:c.70G= NP_001278964.1:p.Gly24=
NM_001369506.1:c.166G= NP_001356435.1:p.Gly56=
NM_015093.6:c.166G= NP_055908.1:p.Gly56=