Canonical Allele Identifier: CA546420477

Gene: TF

Linked Data

• dbSNP Id: rs1303398245
• gnomAD v2: 3-133475900-G-C
• gnomAD v4: 3-133757056-G-C
• MyVariant Identifiers: chr3:g.133475900G>C (hg19) ; chr3:g.133757056G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757056G>C , CM000665.2:g.133757056G>C	GRCh38
NC_000003.11:g.133475900G>C , CM000665.1:g.133475900G>C	GRCh37
NC_000003.10:g.134958590G>C	NCBI36
NG_013080.1:g.15924G>C
NG_013080.2:g.100059G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+47G>C MANE Select	ENSP00000385834.3:n.870+47G>C
ENST00000402696.7:c.870+47G>C	ENSP00000385834.3:n.870+47G>C
ENST00000485977.1:c.235+47G>C	ENSP00000418716.1:n.235+47G>C
NM_001063.3:c.870+47G>C	NP_001054.1:n.870+47G>C
XM_011513100.1:c.870+47G>C	XP_011511402.1:n.870+47G>C
NM_001354703.1:c.738+47G>C	NP_001341632.1:n.738+47G>C
NM_001354704.1:c.489+47G>C	NP_001341633.1:n.489+47G>C
NM_001063.4:c.870+47G>C MANE Select	NP_001054.2:n.870+47G>C
NM_001354703.2:c.738+47G>C	NP_001341632.2:n.738+47G>C
NM_001354704.2:c.489+47G>C	NP_001341633.2:n.489+47G>C