Canonical Allele Identifier: CA899193498

Gene: TF

Linked Data

• dbSNP Id: rs537597598
• gnomAD v3: 3-133757208-G-C
• gnomAD v4: 3-133757208-G-C
• MyVariant Identifiers: chr3:g.133476052G>C (hg19) ; chr3:g.133757208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757208G>C , CM000665.2:g.133757208G>C	GRCh38
NC_000003.11:g.133476052G>C , CM000665.1:g.133476052G>C	GRCh37
NC_000003.10:g.134958742G>C	NCBI36
NG_013080.1:g.16076G>C
NG_013080.2:g.100211G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+199G>C MANE Select	ENSP00000385834.3:n.870+199G>C
ENST00000402696.7:c.870+199G>C	ENSP00000385834.3:n.870+199G>C
ENST00000485977.1:c.235+199G>C	ENSP00000418716.1:n.235+199G>C
NM_001063.3:c.870+199G>C	NP_001054.1:n.870+199G>C
XM_011513100.1:c.870+199G>C	XP_011511402.1:n.870+199G>C
NM_001354703.1:c.738+199G>C	NP_001341632.1:n.738+199G>C
NM_001354704.1:c.489+199G>C	NP_001341633.1:n.489+199G>C
NM_001063.4:c.870+199G>C MANE Select	NP_001054.2:n.870+199G>C
NM_001354703.2:c.738+199G>C	NP_001341632.2:n.738+199G>C
NM_001354704.2:c.489+199G>C	NP_001341633.2:n.489+199G>C