Canonical Allele Identifier: CA386869687
Gene: TBX3 HGNC NCBI

Linked Data

dbSNP Id: rs1483156589

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.114674808T>A , CM000674.2:g.114674808T>A GRCh38
NC_000012.11:g.115112613T>A , CM000674.1:g.115112613T>A GRCh37
NC_000012.10:g.113596996T>A NCBI36
NG_008315.1:g.14357A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349155.7:c.1067A>T MANE Select ENSP00000257567.2:p.Asp356Val
ENST00000257566.7:c.1127A>T ENSP00000257566.3:p.Asp376Val
ENST00000349155.6:c.1067A>T ENSP00000257567.2:p.Asp356Val
ENST00000613550.1:c.1067A>T ENSP00000480048.1:p.Asp356Val
NM_005996.3:c.1067A>T NP_005987.3:p.Asp356Val
NM_016569.3:c.1127A>T NP_057653.3:p.Asp376Val
NM_005996.4:c.1067A>T MANE Select NP_005987.3:p.Asp356Val
NM_016569.4:c.1127A>T NP_057653.3:p.Asp376Val