Canonical Allele Identifier: CA83693146

Gene: TF

Linked Data

• dbSNP Id: rs573152166
• gnomAD v3: 3-133775703-A-T
• gnomAD v4: 3-133775703-A-T
• MyVariant Identifiers: chr3:g.133494547A>T (hg19) ; chr3:g.133775703A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775703A>T , CM000665.2:g.133775703A>T	GRCh38
NC_000003.11:g.133494547A>T , CM000665.1:g.133494547A>T	GRCh37
NC_000003.10:g.134977237A>T	NCBI36
NG_013080.1:g.34571A>T
NG_013080.2:g.118706A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+86A>T MANE Select	ENSP00000385834.3:n.1872+86A>T
ENST00000402696.7:c.1872+86A>T	ENSP00000385834.3:n.1872+86A>T
ENST00000461695.1:c.603+86A>T
ENST00000467842.1:n.2866+86A>T
NM_001063.3:c.1872+86A>T	NP_001054.1:n.1872+86A>T
XM_011513100.1:c.1872+86A>T	XP_011511402.1:n.1872+86A>T
NM_001354703.1:c.1740+86A>T	NP_001341632.1:n.1740+86A>T
NM_001354704.1:c.1491+86A>T	NP_001341633.1:n.1491+86A>T
NM_001063.4:c.1872+86A>T MANE Select	NP_001054.2:n.1872+86A>T
NM_001354703.2:c.1740+86A>T	NP_001341632.2:n.1740+86A>T
NM_001354704.2:c.1491+86A>T	NP_001341633.2:n.1491+86A>T