Canonical Allele Identifier: CA386869741
Gene: TBX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674832A>G , CM000674.2:g.114674832A>G GRCh38
NC_000012.11:g.115112637A>G , CM000674.1:g.115112637A>G GRCh37
NC_000012.10:g.113597020A>G NCBI36
NG_008315.1:g.14333T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1043T>C MANE Select ENSP00000257567.2:p.Leu348Ser
ENST00000257566.7:c.1103T>C ENSP00000257566.3:p.Leu368Ser
ENST00000349155.6:c.1043T>C ENSP00000257567.2:p.Leu348Ser
ENST00000613550.1:c.1043T>C ENSP00000480048.1:p.Leu348Ser
NM_005996.3:c.1043T>C NP_005987.3:p.Leu348Ser
NM_016569.3:c.1103T>C NP_057653.3:p.Leu368Ser
NM_005996.4:c.1043T>C MANE Select NP_005987.3:p.Leu348Ser
NM_016569.4:c.1103T>C NP_057653.3:p.Leu368Ser