Canonical Allele Identifier: CA386869406

Gene: TBX3

Linked Data

• gnomAD v4: 12-114674676-T-G
• MyVariant Identifiers: chr12:g.115112481T>G (hg19) ; chr12:g.114674676T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114674676T>G , CM000674.2:g.114674676T>G	GRCh38
NC_000012.11:g.115112481T>G , CM000674.1:g.115112481T>G	GRCh37
NC_000012.10:g.113596864T>G	NCBI36
NG_008315.1:g.14489A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349155.7:c.1199A>C MANE Select	ENSP00000257567.2:p.Glu400Ala
ENST00000257566.7:c.1259A>C	ENSP00000257566.3:p.Glu420Ala
ENST00000349155.6:c.1199A>C	ENSP00000257567.2:p.Glu400Ala
ENST00000613550.1:c.1199A>C	ENSP00000480048.1:p.Glu400Ala
NM_005996.3:c.1199A>C	NP_005987.3:p.Glu400Ala
NM_016569.3:c.1259A>C	NP_057653.3:p.Glu420Ala
NM_005996.4:c.1199A>C MANE Select	NP_005987.3:p.Glu400Ala
NM_016569.4:c.1259A>C	NP_057653.3:p.Glu420Ala