Canonical Allele Identifier: CA2667769426

Gene: TF

Linked Data

• gnomAD v4: 3-133766211-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766211A>G , CM000665.2:g.133766211A>G	GRCh38
NC_000003.11:g.133485055A>G , CM000665.1:g.133485055A>G	GRCh37
NC_000003.10:g.134967745A>G	NCBI36
NG_013080.1:g.25079A>G
NG_013080.2:g.109214A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1331-67A>G MANE Select	ENSP00000385834.3:n.1331-67A>G
ENST00000402696.7:c.1331-67A>G	ENSP00000385834.3:n.1331-67A>G
NM_001063.3:c.1331-67A>G	NP_001054.1:n.1331-67A>G
XM_011513100.1:c.1331-67A>G	XP_011511402.1:n.1331-67A>G
NM_001354703.1:c.1199-67A>G	NP_001341632.1:n.1199-67A>G
NM_001354704.1:c.950-67A>G	NP_001341633.1:n.950-67A>G
NM_001063.4:c.1331-67A>G MANE Select	NP_001054.2:n.1331-67A>G
NM_001354703.2:c.1199-67A>G	NP_001341632.2:n.1199-67A>G
NM_001354704.2:c.950-67A>G	NP_001341633.2:n.950-67A>G