Canonical Allele Identifier: CA1671915880
Gene: TAB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149379020A= , CM000668.2:g.149379020A= GRCh38
NC_000006.11:g.149700156A= , CM000668.1:g.149700156A= GRCh37
NC_000006.10:g.149741849A= NCBI36
NG_021386.1:g.65721A=
NG_021386.2:g.166097A=

Transcript Alleles

HGVS Amino-acid change
ENST00000703212.1:n.1520A=
ENST00000703213.1:c.1105A= ENSP00000515239.1:p.Ile369=
ENST00000636456.1:c.253A= ENSP00000490379.1:p.Ile85=
ENST00000637181.2:c.1105A= MANE Select ENSP00000490618.1:p.Ile369=
ENST00000367456.5:c.1105A= ENSP00000356426.1:p.Ile369=
ENST00000470466.5:c.1105A= ENSP00000432709.1:p.Ile369=
ENST00000538427.5:c.1105A= ENSP00000445752.1:p.Ile369=
NM_001292034.2:c.1105A= NP_001278963.1:p.Ile369=
NM_001292035.2:c.1009A= NP_001278964.1:p.Ile337=
NM_015093.5:c.1105A= NP_055908.1:p.Ile369=
XM_006715403.2:c.1105A= XP_006715466.1:p.Ile369=
XM_011535633.1:c.1105A= XP_011533935.1:p.Ile369=
XM_011535634.1:c.1105A= XP_011533936.1:p.Ile369=
XM_011535633.2:c.1105A= XP_011533935.1:p.Ile369=
XM_017010591.1:c.1105A= XP_016866080.1:p.Ile369=
XM_017010592.2:c.1105A= XP_016866081.1:p.Ile369=
NM_001292034.3:c.1105A= MANE Select NP_001278963.1:p.Ile369=
NM_001292035.3:c.1009A= NP_001278964.1:p.Ile337=
NM_001369506.1:c.1105A= NP_001356435.1:p.Ile369=
NM_015093.6:c.1105A= NP_055908.1:p.Ile369=