Canonical Allele Identifier: CA365992979
Gene: TAB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149378085A>T , CM000668.2:g.149378085A>T GRCh38
NC_000006.11:g.149699221A>T , CM000668.1:g.149699221A>T GRCh37
NC_000006.10:g.149740914A>T NCBI36
NG_021386.1:g.64786A>T
NG_021386.2:g.165162A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000703212.1:n.585A>T
ENST00000703213.1:c.170A>T ENSP00000515239.1:p.Glu57Val
ENST00000636456.1:c.-96-587A>T ENSP00000490379.1:n.-96-587A>T
ENST00000637181.2:c.170A>T MANE Select ENSP00000490618.1:p.Glu57Val
ENST00000367456.5:c.170A>T ENSP00000356426.1:p.Glu57Val
ENST00000470466.5:c.170A>T ENSP00000432709.1:p.Glu57Val
ENST00000538427.5:c.170A>T ENSP00000445752.1:p.Glu57Val
ENST00000606202.1:c.-53A>T ENSP00000476139.1:n.-53A>T
NM_001292034.2:c.170A>T NP_001278963.1:p.Glu57Val
NM_001292035.2:c.74A>T NP_001278964.1:p.Glu25Val
NM_015093.5:c.170A>T NP_055908.1:p.Glu57Val
XM_006715403.2:c.170A>T XP_006715466.1:p.Glu57Val
XM_011535633.1:c.170A>T XP_011533935.1:p.Glu57Val
XM_011535634.1:c.170A>T XP_011533936.1:p.Glu57Val
XM_011535633.2:c.170A>T XP_011533935.1:p.Glu57Val
XM_017010591.1:c.170A>T XP_016866080.1:p.Glu57Val
XM_017010592.2:c.170A>T XP_016866081.1:p.Glu57Val
NM_001292034.3:c.170A>T MANE Select NP_001278963.1:p.Glu57Val
NM_001292035.3:c.74A>T NP_001278964.1:p.Glu25Val
NM_001369506.1:c.170A>T NP_001356435.1:p.Glu57Val
NM_015093.6:c.170A>T NP_055908.1:p.Glu57Val