Canonical Allele Identifier: CA83692489

Gene: TF

Linked Data

• dbSNP Id: rs558180264
• gnomAD v2: 3-133494080-C-G
• gnomAD v3: 3-133775236-C-G
• gnomAD v4: 3-133775236-C-G
• MyVariant Identifiers: chr3:g.133494080C>G (hg19) ; chr3:g.133775236C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775236C>G , CM000665.2:g.133775236C>G	GRCh38
NC_000003.11:g.133494080C>G , CM000665.1:g.133494080C>G	GRCh37
NC_000003.10:g.134976770C>G	NCBI36
NG_013080.1:g.34104C>G
NG_013080.2:g.118239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-197C>G MANE Select	ENSP00000385834.3:n.1688-197C>G
ENST00000402696.7:c.1688-197C>G	ENSP00000385834.3:n.1688-197C>G
ENST00000461695.1:c.419-197C>G
ENST00000467842.1:n.2485C>G
NM_001063.3:c.1688-197C>G	NP_001054.1:n.1688-197C>G
XM_011513100.1:c.1688-197C>G	XP_011511402.1:n.1688-197C>G
NM_001354703.1:c.1556-197C>G	NP_001341632.1:n.1556-197C>G
NM_001354704.1:c.1307-197C>G	NP_001341633.1:n.1307-197C>G
NM_001063.4:c.1688-197C>G MANE Select	NP_001054.2:n.1688-197C>G
NM_001354703.2:c.1556-197C>G	NP_001341632.2:n.1556-197C>G
NM_001354704.2:c.1307-197C>G	NP_001341633.2:n.1307-197C>G