Canonical Allele Identifier: CA482136554
Gene: TBX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.115112402A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674597A>T , CM000674.2:g.114674597A>T GRCh38
NC_000012.11:g.115112402A>T , CM000674.1:g.115112402A>T GRCh37
NC_000012.10:g.113596785A>T NCBI36
NG_008315.1:g.14568T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1278T>A MANE Select ENSP00000257567.2:p.Thr426=
ENST00000257566.7:c.1338T>A ENSP00000257566.3:p.Thr446=
ENST00000349155.6:c.1278T>A ENSP00000257567.2:p.Thr426=
ENST00000613550.1:c.1278T>A ENSP00000480048.1:p.Thr426=
NM_005996.3:c.1278T>A NP_005987.3:p.Thr426=
NM_016569.3:c.1338T>A NP_057653.3:p.Thr446=
NM_005996.4:c.1278T>A MANE Select NP_005987.3:p.Thr426=
NM_016569.4:c.1338T>A NP_057653.3:p.Thr446=