Canonical Allele Identifier: CA2625400

Gene: TF

Linked Data

• dbSNP Id: rs776581822
• ExAC: 3:133494293 A / G
• gnomAD v2: 3-133494293-A-G
• gnomAD v4: 3-133775449-A-G
• MyVariant Identifiers: chr3:g.133494293A>G (hg19) ; chr3:g.133775449A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775449A>G , CM000665.2:g.133775449A>G	GRCh38
NC_000003.11:g.133494293A>G , CM000665.1:g.133494293A>G	GRCh37
NC_000003.10:g.134976983A>G	NCBI36
NG_013080.1:g.34317A>G
NG_013080.2:g.118452A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1704A>G MANE Select	ENSP00000385834.3:p.Pro568=
ENST00000402696.7:c.1704A>G	ENSP00000385834.3:p.Pro568=
ENST00000461695.1:c.435A>G
ENST00000467842.1:n.2698A>G
NM_001063.3:c.1704A>G	NP_001054.1:p.Pro568=
XM_011513100.1:c.1704A>G	XP_011511402.1:p.Pro568=
NM_001354703.1:c.1572A>G	NP_001341632.1:p.Pro524=
NM_001354704.1:c.1323A>G	NP_001341633.1:p.Pro441=
NM_001063.4:c.1704A>G MANE Select	NP_001054.2:p.Pro568=
NM_001354703.2:c.1572A>G	NP_001341632.2:p.Pro524=
NM_001354704.2:c.1323A>G	NP_001341633.2:p.Pro441=