Canonical Allele Identifier: CA354610358

Gene: TF

Linked Data

• dbSNP Id: rs1376049125
• gnomAD v2: 3-133494355-C-G
• gnomAD v4: 3-133775511-C-G
• MyVariant Identifiers: chr3:g.133494355C>G (hg19) ; chr3:g.133775511C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775511C>G , CM000665.2:g.133775511C>G	GRCh38
NC_000003.11:g.133494355C>G , CM000665.1:g.133494355C>G	GRCh37
NC_000003.10:g.134977045C>G	NCBI36
NG_013080.1:g.34379C>G
NG_013080.2:g.118514C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1766C>G MANE Select	ENSP00000385834.3:p.Pro589Arg
ENST00000402696.7:c.1766C>G	ENSP00000385834.3:p.Pro589Arg
ENST00000461695.1:c.497C>G
ENST00000467842.1:n.2760C>G
NM_001063.3:c.1766C>G	NP_001054.1:p.Pro589Arg
XM_011513100.1:c.1766C>G	XP_011511402.1:p.Pro589Arg
NM_001354703.1:c.1634C>G	NP_001341632.1:p.Pro545Arg
NM_001354704.1:c.1385C>G	NP_001341633.1:p.Pro462Arg
NM_001063.4:c.1766C>G MANE Select	NP_001054.2:p.Pro589Arg
NM_001354703.2:c.1634C>G	NP_001341632.2:p.Pro545Arg
NM_001354704.2:c.1385C>G	NP_001341633.2:p.Pro462Arg