Canonical Allele Identifier: CA83674650

Gene: TF

Linked Data

• dbSNP Id: rs552051384
• gnomAD v3: 3-133757090-C-A
• gnomAD v4: 3-133757090-C-A
• MyVariant Identifiers: chr3:g.133475934C>A (hg19) ; chr3:g.133757090C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757090C>A , CM000665.2:g.133757090C>A	GRCh38
NC_000003.11:g.133475934C>A , CM000665.1:g.133475934C>A	GRCh37
NC_000003.10:g.134958624C>A	NCBI36
NG_013080.1:g.15958C>A
NG_013080.2:g.100093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+81C>A MANE Select	ENSP00000385834.3:n.870+81C>A
ENST00000402696.7:c.870+81C>A	ENSP00000385834.3:n.870+81C>A
ENST00000485977.1:c.235+81C>A	ENSP00000418716.1:n.235+81C>A
NM_001063.3:c.870+81C>A	NP_001054.1:n.870+81C>A
XM_011513100.1:c.870+81C>A	XP_011511402.1:n.870+81C>A
NM_001354703.1:c.738+81C>A	NP_001341632.1:n.738+81C>A
NM_001354704.1:c.489+81C>A	NP_001341633.1:n.489+81C>A
NM_001063.4:c.870+81C>A MANE Select	NP_001054.2:n.870+81C>A
NM_001354703.2:c.738+81C>A	NP_001341632.2:n.738+81C>A
NM_001354704.2:c.489+81C>A	NP_001341633.2:n.489+81C>A