Canonical Allele Identifier: CA386869598
Gene: TBX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674767A>T , CM000674.2:g.114674767A>T GRCh38
NC_000012.11:g.115112572A>T , CM000674.1:g.115112572A>T GRCh37
NC_000012.10:g.113596955A>T NCBI36
NG_008315.1:g.14398T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1108T>A MANE Select ENSP00000257567.2:p.Cys370Ser
ENST00000257566.7:c.1168T>A ENSP00000257566.3:p.Cys390Ser
ENST00000349155.6:c.1108T>A ENSP00000257567.2:p.Cys370Ser
ENST00000613550.1:c.1108T>A ENSP00000480048.1:p.Cys370Ser
NM_005996.3:c.1108T>A NP_005987.3:p.Cys370Ser
NM_016569.3:c.1168T>A NP_057653.3:p.Cys390Ser
NM_005996.4:c.1108T>A MANE Select NP_005987.3:p.Cys370Ser
NM_016569.4:c.1168T>A NP_057653.3:p.Cys390Ser