Canonical Allele Identifier: CA386869677

Gene: TBX3

Linked Data

• gnomAD v4: 12-114674803-C-A
• MyVariant Identifiers: chr12:g.115112608C>A (hg19) ; chr12:g.114674803C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674803C>A , CM000674.2:g.114674803C>A	GRCh38
NC_000012.11:g.115112608C>A , CM000674.1:g.115112608C>A	GRCh37
NC_000012.10:g.113596991C>A	NCBI36
NG_008315.1:g.14362G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1072G>T MANE Select	ENSP00000257567.2:p.Glu358Ter
ENST00000257566.7:c.1132G>T	ENSP00000257566.3:p.Glu378Ter
ENST00000349155.6:c.1072G>T	ENSP00000257567.2:p.Glu358Ter
ENST00000613550.1:c.1072G>T	ENSP00000480048.1:p.Glu358Ter
NM_005996.3:c.1072G>T	NP_005987.3:p.Glu358Ter
NM_016569.3:c.1132G>T	NP_057653.3:p.Glu378Ter
NM_005996.4:c.1072G>T MANE Select	NP_005987.3:p.Glu358Ter
NM_016569.4:c.1132G>T	NP_057653.3:p.Glu378Ter