Canonical Allele Identifier: CA1671914690
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149378083T= , CM000668.2:g.149378083T= GRCh38
NC_000006.11:g.149699219T= , CM000668.1:g.149699219T= GRCh37
NC_000006.10:g.149740912T= NCBI36
NG_021386.1:g.64784T=
NG_021386.2:g.165160T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.583T=
ENST00000703213.1:c.168T= ENSP00000515239.1:p.Gly56=
ENST00000636456.1:c.-96-589T= ENSP00000490379.1:n.-96-589T=
ENST00000637181.2:c.168T= MANE Select ENSP00000490618.1:p.Gly56=
ENST00000367456.5:c.168T= ENSP00000356426.1:p.Gly56=
ENST00000470466.5:c.168T= ENSP00000432709.1:p.Gly56=
ENST00000538427.5:c.168T= ENSP00000445752.1:p.Gly56=
ENST00000606202.1:c.-55T= ENSP00000476139.1:n.-55T=
NM_001292034.2:c.168T= NP_001278963.1:p.Gly56=
NM_001292035.2:c.72T= NP_001278964.1:p.Gly24=
NM_015093.5:c.168T= NP_055908.1:p.Gly56=
XM_006715403.2:c.168T= XP_006715466.1:p.Gly56=
XM_011535633.1:c.168T= XP_011533935.1:p.Gly56=
XM_011535634.1:c.168T= XP_011533936.1:p.Gly56=
XM_011535633.2:c.168T= XP_011533935.1:p.Gly56=
XM_017010591.1:c.168T= XP_016866080.1:p.Gly56=
XM_017010592.2:c.168T= XP_016866081.1:p.Gly56=
NM_001292034.3:c.168T= MANE Select NP_001278963.1:p.Gly56=
NM_001292035.3:c.72T= NP_001278964.1:p.Gly24=
NM_001369506.1:c.168T= NP_001356435.1:p.Gly56=
NM_015093.6:c.168T= NP_055908.1:p.Gly56=