Canonical Allele Identifier: CA482136769

Gene: TBX3

Linked Data

• MyVariant Identifiers: chr12:g.115112474G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674669G>A , CM000674.2:g.114674669G>A	GRCh38
NC_000012.11:g.115112474G>A , CM000674.1:g.115112474G>A	GRCh37
NC_000012.10:g.113596857G>A	NCBI36
NG_008315.1:g.14496C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1206C>T MANE Select	ENSP00000257567.2:p.Pro402=
ENST00000257566.7:c.1266C>T	ENSP00000257566.3:p.Pro422=
ENST00000349155.6:c.1206C>T	ENSP00000257567.2:p.Pro402=
ENST00000613550.1:c.1206C>T	ENSP00000480048.1:p.Pro402=
NM_005996.3:c.1206C>T	NP_005987.3:p.Pro402=
NM_016569.3:c.1266C>T	NP_057653.3:p.Pro422=
NM_005996.4:c.1206C>T MANE Select	NP_005987.3:p.Pro402=
NM_016569.4:c.1266C>T	NP_057653.3:p.Pro422=