Canonical Allele Identifier: CA2064766477
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674624A= , CM000674.2:g.114674624A= GRCh38
NC_000012.11:g.115112429A= , CM000674.1:g.115112429A= GRCh37
NC_000012.10:g.113596812A= NCBI36
NG_008315.1:g.14541T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1251T= MANE Select ENSP00000257567.2:p.His417=
ENST00000257566.7:c.1311T= ENSP00000257566.3:p.His437=
ENST00000349155.6:c.1251T= ENSP00000257567.2:p.His417=
ENST00000613550.1:c.1251T= ENSP00000480048.1:p.His417=
NM_005996.3:c.1251T= NP_005987.3:p.His417=
NM_016569.3:c.1311T= NP_057653.3:p.His437=
NM_005996.4:c.1251T= MANE Select NP_005987.3:p.His417=
NM_016569.4:c.1311T= NP_057653.3:p.His437=