Canonical Allele Identifier: CA2064766428
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674596G= , CM000674.2:g.114674596G= GRCh38
NC_000012.11:g.115112401G= , CM000674.1:g.115112401G= GRCh37
NC_000012.10:g.113596784G= NCBI36
NG_008315.1:g.14569C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1279C= MANE Select ENSP00000257567.2:p.Arg427=
ENST00000257566.7:c.1339C= ENSP00000257566.3:p.Arg447=
ENST00000349155.6:c.1279C= ENSP00000257567.2:p.Arg427=
ENST00000613550.1:c.1279C= ENSP00000480048.1:p.Arg427=
NM_005996.3:c.1279C= NP_005987.3:p.Arg427=
NM_016569.3:c.1339C= NP_057653.3:p.Arg447=
NM_005996.4:c.1279C= MANE Select NP_005987.3:p.Arg427=
NM_016569.4:c.1339C= NP_057653.3:p.Arg447=