Canonical Allele Identifier: CA386869379

Gene: TBX3

Linked Data

• MyVariant Identifiers: chr12:g.115112466C>G (hg19) ; chr12:g.114674661C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674661C>G , CM000674.2:g.114674661C>G	GRCh38
NC_000012.11:g.115112466C>G , CM000674.1:g.115112466C>G	GRCh37
NC_000012.10:g.113596849C>G	NCBI36
NG_008315.1:g.14504G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1214G>C MANE Select	ENSP00000257567.2:p.Ser405Thr
ENST00000257566.7:c.1274G>C	ENSP00000257566.3:p.Ser425Thr
ENST00000349155.6:c.1214G>C	ENSP00000257567.2:p.Ser405Thr
ENST00000613550.1:c.1214G>C	ENSP00000480048.1:p.Ser405Thr
NM_005996.3:c.1214G>C	NP_005987.3:p.Ser405Thr
NM_016569.3:c.1274G>C	NP_057653.3:p.Ser425Thr
NM_005996.4:c.1214G>C MANE Select	NP_005987.3:p.Ser405Thr
NM_016569.4:c.1274G>C	NP_057653.3:p.Ser425Thr