Canonical Allele Identifier: CA2625118

Gene: TF

Linked Data

• dbSNP Id: rs531769552
• ExAC: 3:133475879 C / G
• gnomAD v2: 3-133475879-C-G
• gnomAD v3: 3-133757035-C-G
• gnomAD v4: 3-133757035-C-G
• MyVariant Identifiers: chr3:g.133475879C>G (hg19) ; chr3:g.133757035C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757035C>G , CM000665.2:g.133757035C>G	GRCh38
NC_000003.11:g.133475879C>G , CM000665.1:g.133475879C>G	GRCh37
NC_000003.10:g.134958569C>G	NCBI36
NG_013080.1:g.15903C>G
NG_013080.2:g.100038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+26C>G MANE Select	ENSP00000385834.3:n.870+26C>G
ENST00000402696.7:c.870+26C>G	ENSP00000385834.3:n.870+26C>G
ENST00000485977.1:c.235+26C>G	ENSP00000418716.1:n.235+26C>G
NM_001063.3:c.870+26C>G	NP_001054.1:n.870+26C>G
XM_011513100.1:c.870+26C>G	XP_011511402.1:n.870+26C>G
NM_001354703.1:c.738+26C>G	NP_001341632.1:n.738+26C>G
NM_001354704.1:c.489+26C>G	NP_001341633.1:n.489+26C>G
NM_001063.4:c.870+26C>G MANE Select	NP_001054.2:n.870+26C>G
NM_001354703.2:c.738+26C>G	NP_001341632.2:n.738+26C>G
NM_001354704.2:c.489+26C>G	NP_001341633.2:n.489+26C>G