Canonical Allele Identifier: CA386869668

Gene: TBX3

Linked Data

• gnomAD v4: 12-114674799-G-T
• MyVariant Identifiers: chr12:g.115112604G>T (hg19) ; chr12:g.114674799G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674799G>T , CM000674.2:g.114674799G>T	GRCh38
NC_000012.11:g.115112604G>T , CM000674.1:g.115112604G>T	GRCh37
NC_000012.10:g.113596987G>T	NCBI36
NG_008315.1:g.14366C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1076C>A MANE Select	ENSP00000257567.2:p.Ala359Asp
ENST00000257566.7:c.1136C>A	ENSP00000257566.3:p.Ala379Asp
ENST00000349155.6:c.1076C>A	ENSP00000257567.2:p.Ala359Asp
ENST00000613550.1:c.1076C>A	ENSP00000480048.1:p.Ala359Asp
NM_005996.3:c.1076C>A	NP_005987.3:p.Ala359Asp
NM_016569.3:c.1136C>A	NP_057653.3:p.Ala379Asp
NM_005996.4:c.1076C>A MANE Select	NP_005987.3:p.Ala359Asp
NM_016569.4:c.1136C>A	NP_057653.3:p.Ala379Asp