Canonical Allele Identifier: CA2625394

Gene: TF

Linked Data

• dbSNP Id: rs8177302
• ExAC: 3:133494238 C / A
• gnomAD v2: 3-133494238-C-A
• gnomAD v3: 3-133775394-C-A
• gnomAD v4: 3-133775394-C-A
• MyVariant Identifiers: chr3:g.133494238C>A (hg19) ; chr3:g.133775394C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775394C>A , CM000665.2:g.133775394C>A	GRCh38
NC_000003.11:g.133494238C>A , CM000665.1:g.133494238C>A	GRCh37
NC_000003.10:g.134976928C>A	NCBI36
NG_013080.1:g.34262C>A
NG_013080.2:g.118397C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-39C>A MANE Select	ENSP00000385834.3:n.1688-39C>A
ENST00000402696.7:c.1688-39C>A	ENSP00000385834.3:n.1688-39C>A
ENST00000461695.1:c.419-39C>A
ENST00000467842.1:n.2643C>A
NM_001063.3:c.1688-39C>A	NP_001054.1:n.1688-39C>A
XM_011513100.1:c.1688-39C>A	XP_011511402.1:n.1688-39C>A
NM_001354703.1:c.1556-39C>A	NP_001341632.1:n.1556-39C>A
NM_001354704.1:c.1307-39C>A	NP_001341633.1:n.1307-39C>A
NM_001063.4:c.1688-39C>A MANE Select	NP_001054.2:n.1688-39C>A
NM_001354703.2:c.1556-39C>A	NP_001341632.2:n.1556-39C>A
NM_001354704.2:c.1307-39C>A	NP_001341633.2:n.1307-39C>A