Canonical Allele Identifier: CA435815835

Gene: TF

Linked Data

• dbSNP Id: rs1467911192
• gnomAD v3: 3-133775506-G-A
• gnomAD v4: 3-133775506-G-A
• MyVariant Identifiers: chr3:g.133494350G>A (hg19) ; chr3:g.133775506G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775506G>A , CM000665.2:g.133775506G>A	GRCh38
NC_000003.11:g.133494350G>A , CM000665.1:g.133494350G>A	GRCh37
NC_000003.10:g.134977040G>A	NCBI36
NG_013080.1:g.34374G>A
NG_013080.2:g.118509G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1761G>A MANE Select	ENSP00000385834.3:p.Arg587=
ENST00000402696.7:c.1761G>A	ENSP00000385834.3:p.Arg587=
ENST00000461695.1:c.492G>A
ENST00000467842.1:n.2755G>A
NM_001063.3:c.1761G>A	NP_001054.1:p.Arg587=
XM_011513100.1:c.1761G>A	XP_011511402.1:p.Arg587=
NM_001354703.1:c.1629G>A	NP_001341632.1:p.Arg543=
NM_001354704.1:c.1380G>A	NP_001341633.1:p.Arg460=
NM_001063.4:c.1761G>A MANE Select	NP_001054.2:p.Arg587=
NM_001354703.2:c.1629G>A	NP_001341632.2:p.Arg543=
NM_001354704.2:c.1380G>A	NP_001341633.2:p.Arg460=