Canonical Allele Identifier: CA2625120

Gene: TF

Linked Data

• dbSNP Id: rs758017678
• ExAC: 3:133475899 T / G
• gnomAD v2: 3-133475899-T-G
• gnomAD v3: 3-133757055-T-G
• gnomAD v4: 3-133757055-T-G
• MyVariant Identifiers: chr3:g.133475899T>G (hg19) ; chr3:g.133757055T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757055T>G , CM000665.2:g.133757055T>G	GRCh38
NC_000003.11:g.133475899T>G , CM000665.1:g.133475899T>G	GRCh37
NC_000003.10:g.134958589T>G	NCBI36
NG_013080.1:g.15923T>G
NG_013080.2:g.100058T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+46T>G MANE Select	ENSP00000385834.3:n.870+46T>G
ENST00000402696.7:c.870+46T>G	ENSP00000385834.3:n.870+46T>G
ENST00000485977.1:c.235+46T>G	ENSP00000418716.1:n.235+46T>G
NM_001063.3:c.870+46T>G	NP_001054.1:n.870+46T>G
XM_011513100.1:c.870+46T>G	XP_011511402.1:n.870+46T>G
NM_001354703.1:c.738+46T>G	NP_001341632.1:n.738+46T>G
NM_001354704.1:c.489+46T>G	NP_001341633.1:n.489+46T>G
NM_001063.4:c.870+46T>G MANE Select	NP_001054.2:n.870+46T>G
NM_001354703.2:c.738+46T>G	NP_001341632.2:n.738+46T>G
NM_001354704.2:c.489+46T>G	NP_001341633.2:n.489+46T>G