Canonical Allele Identifier: CA83685462

Gene: TF

Linked Data

• dbSNP Id: rs1049087990
• gnomAD v4: 3-133766253-T-G
• MyVariant Identifiers: chr3:g.133485097T>G (hg19) ; chr3:g.133766253T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766253T>G , CM000665.2:g.133766253T>G	GRCh38
NC_000003.11:g.133485097T>G , CM000665.1:g.133485097T>G	GRCh37
NC_000003.10:g.134967787T>G	NCBI36
NG_013080.1:g.25121T>G
NG_013080.2:g.109256T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1331-25T>G MANE Select	ENSP00000385834.3:n.1331-25T>G
ENST00000402696.7:c.1331-25T>G	ENSP00000385834.3:n.1331-25T>G
NM_001063.3:c.1331-25T>G	NP_001054.1:n.1331-25T>G
XM_011513100.1:c.1331-25T>G	XP_011511402.1:n.1331-25T>G
NM_001354703.1:c.1199-25T>G	NP_001341632.1:n.1199-25T>G
NM_001354704.1:c.950-25T>G	NP_001341633.1:n.950-25T>G
NM_001063.4:c.1331-25T>G MANE Select	NP_001054.2:n.1331-25T>G
NM_001354703.2:c.1199-25T>G	NP_001341632.2:n.1199-25T>G
NM_001354704.2:c.950-25T>G	NP_001341633.2:n.950-25T>G