Canonical Allele Identifier: CA2064766587
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674674G= , CM000674.2:g.114674674G= GRCh38
NC_000012.11:g.115112479G= , CM000674.1:g.115112479G= GRCh37
NC_000012.10:g.113596862G= NCBI36
NG_008315.1:g.14491C=

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.1201C= MANE Select ENSP00000257567.2:p.Arg401=
ENST00000257566.7:c.1261C= ENSP00000257566.3:p.Arg421=
ENST00000349155.6:c.1201C= ENSP00000257567.2:p.Arg401=
ENST00000613550.1:c.1201C= ENSP00000480048.1:p.Arg401=
NM_005996.3:c.1201C= NP_005987.3:p.Arg401=
NM_016569.3:c.1261C= NP_057653.3:p.Arg421=
NM_005996.4:c.1201C= MANE Select NP_005987.3:p.Arg401=
NM_016569.4:c.1261C= NP_057653.3:p.Arg421=