Canonical Allele Identifier: CA2064766612
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674685A= , CM000674.2:g.114674685A= GRCh38
NC_000012.11:g.115112490A= , CM000674.1:g.115112490A= GRCh37
NC_000012.10:g.113596873A= NCBI36
NG_008315.1:g.14480T=

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.1190T= MANE Select ENSP00000257567.2:p.Phe397=
ENST00000257566.7:c.1250T= ENSP00000257566.3:p.Phe417=
ENST00000349155.6:c.1190T= ENSP00000257567.2:p.Phe397=
ENST00000613550.1:c.1190T= ENSP00000480048.1:p.Phe397=
NM_005996.3:c.1190T= NP_005987.3:p.Phe397=
NM_016569.3:c.1250T= NP_057653.3:p.Phe417=
NM_005996.4:c.1190T= MANE Select NP_005987.3:p.Phe397=
NM_016569.4:c.1250T= NP_057653.3:p.Phe417=