Canonical Allele Identifier: CA546420586

Gene: TF

Linked Data

• dbSNP Id: rs774406753
• gnomAD v2: 3-133495870-C-T
• gnomAD v3: 3-133777026-C-T
• gnomAD v4: 3-133777026-C-T
• COSMIC: COSN20884589
• MyVariant Identifiers: chr3:g.133495870C>T (hg19) ; chr3:g.133777026C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777026C>T , CM000665.2:g.133777026C>T	GRCh38
NC_000003.11:g.133495870C>T , CM000665.1:g.133495870C>T	GRCh37
NC_000003.10:g.134978560C>T	NCBI36
NG_013080.1:g.35894C>T
NG_013080.2:g.120029C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-23C>T MANE Select	ENSP00000385834.3:n.1873-23C>T
ENST00000402696.7:c.1873-23C>T	ENSP00000385834.3:n.1873-23C>T
ENST00000461695.1:c.604-23C>T
ENST00000467842.1:n.2867-23C>T
NM_001063.3:c.1873-23C>T	NP_001054.1:n.1873-23C>T
XM_011513100.1:c.1873-23C>T	XP_011511402.1:n.1873-23C>T
NM_001354703.1:c.1741-23C>T	NP_001341632.1:n.1741-23C>T
NM_001354704.1:c.1492-23C>T	NP_001341633.1:n.1492-23C>T
NM_001063.4:c.1873-23C>T MANE Select	NP_001054.2:n.1873-23C>T
NM_001354703.2:c.1741-23C>T	NP_001341632.2:n.1741-23C>T
NM_001354704.2:c.1492-23C>T	NP_001341633.2:n.1492-23C>T