Canonical Allele Identifier: CA2064789981
Gene: TBX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114670324A= , CM000674.2:g.114670324A= GRCh38
NC_000012.11:g.115108129A= , CM000674.1:g.115108129A= GRCh37
NC_000012.10:g.113592512A= NCBI36
NG_008315.1:g.18841T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.*1517T= MANE Select ENSP00000257567.2:n.*1517T=
ENST00000257566.7:c.*1517T= ENSP00000257566.3:n.*1517T=
ENST00000349155.6:c.*1517T= ENSP00000257567.2:n.*1517T=
NM_005996.3:c.*1517T= NP_005987.3:n.*1517T=
NM_016569.3:c.*1517T= NP_057653.3:n.*1517T=
NM_005996.4:c.*1517T= MANE Select NP_005987.3:n.*1517T=
NM_016569.4:c.*1517T= NP_057653.3:n.*1517T=