Canonical Allele Identifier: CA899131915

Gene: TF

Linked Data

• dbSNP Id: rs1216067064
• gnomAD v3: 3-133775862-A-C
• gnomAD v4: 3-133775862-A-C
• MyVariant Identifiers: chr3:g.133494706A>C (hg19) ; chr3:g.133775862A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775862A>C , CM000665.2:g.133775862A>C	GRCh38
NC_000003.11:g.133494706A>C , CM000665.1:g.133494706A>C	GRCh37
NC_000003.10:g.134977396A>C	NCBI36
NG_013080.1:g.34730A>C
NG_013080.2:g.118865A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+245A>C MANE Select	ENSP00000385834.3:n.1872+245A>C
ENST00000402696.7:c.1872+245A>C	ENSP00000385834.3:n.1872+245A>C
ENST00000461695.1:c.603+245A>C
ENST00000467842.1:n.2866+245A>C
NM_001063.3:c.1872+245A>C	NP_001054.1:n.1872+245A>C
XM_011513100.1:c.1872+245A>C	XP_011511402.1:n.1872+245A>C
NM_001354703.1:c.1740+245A>C	NP_001341632.1:n.1740+245A>C
NM_001354704.1:c.1491+245A>C	NP_001341633.1:n.1491+245A>C
NM_001063.4:c.1872+245A>C MANE Select	NP_001054.2:n.1872+245A>C
NM_001354703.2:c.1740+245A>C	NP_001341632.2:n.1740+245A>C
NM_001354704.2:c.1491+245A>C	NP_001341633.2:n.1491+245A>C