Canonical Allele Identifier: CA2064759784
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114670560T= , CM000674.2:g.114670560T= GRCh38
NC_000012.11:g.115108365T= , CM000674.1:g.115108365T= GRCh37
NC_000012.10:g.113592748T= NCBI36
NG_008315.1:g.18605A=

Transcript Alleles

HGVS Amino-acid change
ENST00000349155.7:c.*1281A= MANE Select ENSP00000257567.2:n.*1281A=
ENST00000257566.7:c.*1281A= ENSP00000257566.3:n.*1281A=
ENST00000349155.6:c.*1281A= ENSP00000257567.2:n.*1281A=
NM_005996.3:c.*1281A= NP_005987.3:n.*1281A=
NM_016569.3:c.*1281A= NP_057653.3:n.*1281A=
NM_005996.4:c.*1281A= MANE Select NP_005987.3:n.*1281A=
NM_016569.4:c.*1281A= NP_057653.3:n.*1281A=