Canonical Allele Identifier: CA386869709
Gene: TBX3 HGNC NCBI

Linked Data

dbSNP Id: rs769194863

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674817C>T , CM000674.2:g.114674817C>T GRCh38
NC_000012.11:g.115112622C>T , CM000674.1:g.115112622C>T GRCh37
NC_000012.10:g.113597005C>T NCBI36
NG_008315.1:g.14348G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1058G>A MANE Select ENSP00000257567.2:p.Gly353Asp
ENST00000257566.7:c.1118G>A ENSP00000257566.3:p.Gly373Asp
ENST00000349155.6:c.1058G>A ENSP00000257567.2:p.Gly353Asp
ENST00000613550.1:c.1058G>A ENSP00000480048.1:p.Gly353Asp
NM_005996.3:c.1058G>A NP_005987.3:p.Gly353Asp
NM_016569.3:c.1118G>A NP_057653.3:p.Gly373Asp
NM_005996.4:c.1058G>A MANE Select NP_005987.3:p.Gly353Asp
NM_016569.4:c.1118G>A NP_057653.3:p.Gly373Asp