Canonical Allele Identifier: CA2625068

Gene: TF

Linked Data

• dbSNP Id: rs575318531
• ExAC: 3:133475638 C / T
• gnomAD v2: 3-133475638-C-T
• gnomAD v3: 3-133756794-C-T
• gnomAD v4: 3-133756794-C-T
• MyVariant Identifiers: chr3:g.133475638C>T (hg19) ; chr3:g.133756794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756794C>T , CM000665.2:g.133756794C>T	GRCh38
NC_000003.11:g.133475638C>T , CM000665.1:g.133475638C>T	GRCh37
NC_000003.10:g.134958328C>T	NCBI36
NG_013080.1:g.15662C>T
NG_013080.2:g.99797C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.692-37C>T MANE Select	ENSP00000385834.3:n.692-37C>T
ENST00000402696.7:c.692-37C>T	ENSP00000385834.3:n.692-37C>T
ENST00000482271.5:c.311-37C>T	ENSP00000419338.1:n.311-37C>T
ENST00000485977.1:c.158-138C>T	ENSP00000418716.1:n.158-138C>T
NM_001063.3:c.692-37C>T	NP_001054.1:n.692-37C>T
XM_011513100.1:c.692-37C>T	XP_011511402.1:n.692-37C>T
NM_001354703.1:c.560-37C>T	NP_001341632.1:n.560-37C>T
NM_001354704.1:c.311-37C>T	NP_001341633.1:n.311-37C>T
NM_001063.4:c.692-37C>T MANE Select	NP_001054.2:n.692-37C>T
NM_001354703.2:c.560-37C>T	NP_001341632.2:n.560-37C>T
NM_001354704.2:c.311-37C>T	NP_001341633.2:n.311-37C>T