Canonical Allele Identifier: CA83693170

Gene: TF

Linked Data

• dbSNP Id: rs41296600
• MyVariant Identifiers: chr3:g.133494589T>G (hg19) ; chr3:g.133775745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775745T>G , CM000665.2:g.133775745T>G	GRCh38
NC_000003.11:g.133494589T>G , CM000665.1:g.133494589T>G	GRCh37
NC_000003.10:g.134977279T>G	NCBI36
NG_013080.1:g.34613T>G
NG_013080.2:g.118748T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1872+128T>G MANE Select	ENSP00000385834.3:n.1872+128T>G
ENST00000402696.7:c.1872+128T>G	ENSP00000385834.3:n.1872+128T>G
ENST00000461695.1:c.603+128T>G
ENST00000467842.1:n.2866+128T>G
NM_001063.3:c.1872+128T>G	NP_001054.1:n.1872+128T>G
XM_011513100.1:c.1872+128T>G	XP_011511402.1:n.1872+128T>G
NM_001354703.1:c.1740+128T>G	NP_001341632.1:n.1740+128T>G
NM_001354704.1:c.1491+128T>G	NP_001341633.1:n.1491+128T>G
NM_001063.4:c.1872+128T>G MANE Select	NP_001054.2:n.1872+128T>G
NM_001354703.2:c.1740+128T>G	NP_001341632.2:n.1740+128T>G
NM_001354704.2:c.1491+128T>G	NP_001341633.2:n.1491+128T>G