Canonical Allele Identifier: CA365992969
Gene: TAB2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.581G>C
ENST00000703213.1:c.166G>C ENSP00000515239.1:p.Gly56Arg
ENST00000636456.1:c.-96-591G>C ENSP00000490379.1:n.-96-591G>C
ENST00000637181.2:c.166G>C MANE Select ENSP00000490618.1:p.Gly56Arg
ENST00000367456.5:c.166G>C ENSP00000356426.1:p.Gly56Arg
ENST00000470466.5:c.166G>C ENSP00000432709.1:p.Gly56Arg
ENST00000538427.5:c.166G>C ENSP00000445752.1:p.Gly56Arg
ENST00000606202.1:c.-57G>C ENSP00000476139.1:n.-57G>C
NM_001292034.2:c.166G>C NP_001278963.1:p.Gly56Arg
NM_001292035.2:c.70G>C NP_001278964.1:p.Gly24Arg
NM_015093.5:c.166G>C NP_055908.1:p.Gly56Arg
XM_006715403.2:c.166G>C XP_006715466.1:p.Gly56Arg
XM_011535633.1:c.166G>C XP_011533935.1:p.Gly56Arg
XM_011535634.1:c.166G>C XP_011533936.1:p.Gly56Arg
XM_011535633.2:c.166G>C XP_011533935.1:p.Gly56Arg
XM_017010591.1:c.166G>C XP_016866080.1:p.Gly56Arg
XM_017010592.2:c.166G>C XP_016866081.1:p.Gly56Arg
NM_001292034.3:c.166G>C MANE Select NP_001278963.1:p.Gly56Arg
NM_001292035.3:c.70G>C NP_001278964.1:p.Gly24Arg
NM_001369506.1:c.166G>C NP_001356435.1:p.Gly56Arg
NM_015093.6:c.166G>C NP_055908.1:p.Gly56Arg