Canonical Allele Identifier: CA482136613

Gene: TBX3

Linked Data

• dbSNP Id: rs2121384626
• COSMIC: COSM5374287
• MyVariant Identifiers: chr12:g.115112423G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674618G>A , CM000674.2:g.114674618G>A	GRCh38
NC_000012.11:g.115112423G>A , CM000674.1:g.115112423G>A	GRCh37
NC_000012.10:g.113596806G>A	NCBI36
NG_008315.1:g.14547C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1257C>T MANE Select	ENSP00000257567.2:p.Pro419=
ENST00000257566.7:c.1317C>T	ENSP00000257566.3:p.Pro439=
ENST00000349155.6:c.1257C>T	ENSP00000257567.2:p.Pro419=
ENST00000613550.1:c.1257C>T	ENSP00000480048.1:p.Pro419=
NM_005996.3:c.1257C>T	NP_005987.3:p.Pro419=
NM_016569.3:c.1317C>T	NP_057653.3:p.Pro439=
NM_005996.4:c.1257C>T MANE Select	NP_005987.3:p.Pro419=
NM_016569.4:c.1317C>T	NP_057653.3:p.Pro439=