Canonical Allele Identifier: CA2064790033
Gene: TBX3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114670452C= , CM000674.2:g.114670452C= GRCh38
NC_000012.11:g.115108257C= , CM000674.1:g.115108257C= GRCh37
NC_000012.10:g.113592640C= NCBI36
NG_008315.1:g.18713G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.*1389G= MANE Select ENSP00000257567.2:n.*1389G=
ENST00000257566.7:c.*1389G= ENSP00000257566.3:n.*1389G=
ENST00000349155.6:c.*1389G= ENSP00000257567.2:n.*1389G=
NM_005996.3:c.*1389G= NP_005987.3:n.*1389G=
NM_016569.3:c.*1389G= NP_057653.3:n.*1389G=
NM_005996.4:c.*1389G= MANE Select NP_005987.3:n.*1389G=
NM_016569.4:c.*1389G= NP_057653.3:n.*1389G=
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