Canonical Allele Identifier: CA899131831

Gene: TF

Linked Data

• dbSNP Id: rs1417154061
• gnomAD v4: 3-133775673-G-A
• MyVariant Identifiers: chr3:g.133494517G>A (hg19) ; chr3:g.133775673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775673G>A , CM000665.2:g.133775673G>A	GRCh38
NC_000003.11:g.133494517G>A , CM000665.1:g.133494517G>A	GRCh37
NC_000003.10:g.134977207G>A	NCBI36
NG_013080.1:g.34541G>A
NG_013080.2:g.118676G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+56G>A MANE Select	ENSP00000385834.3:n.1872+56G>A
ENST00000402696.7:c.1872+56G>A	ENSP00000385834.3:n.1872+56G>A
ENST00000461695.1:c.603+56G>A
ENST00000467842.1:n.2866+56G>A
NM_001063.3:c.1872+56G>A	NP_001054.1:n.1872+56G>A
XM_011513100.1:c.1872+56G>A	XP_011511402.1:n.1872+56G>A
NM_001354703.1:c.1740+56G>A	NP_001341632.1:n.1740+56G>A
NM_001354704.1:c.1491+56G>A	NP_001341633.1:n.1491+56G>A
NM_001063.4:c.1872+56G>A MANE Select	NP_001054.2:n.1872+56G>A
NM_001354703.2:c.1740+56G>A	NP_001341632.2:n.1740+56G>A
NM_001354704.2:c.1491+56G>A	NP_001341633.2:n.1491+56G>A