Canonical Allele Identifier: CA11538563

Gene: TF

Linked Data

• dbSNP Id: rs8177234
• gnomAD v2: 3-133476050-C-T
• gnomAD v3: 3-133757206-C-T
• gnomAD v4: 3-133757206-C-T
• MyVariant Identifiers: chr3:g.133476050C>T (hg19) ; chr3:g.133757206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757206C>T , CM000665.2:g.133757206C>T	GRCh38
NC_000003.11:g.133476050C>T , CM000665.1:g.133476050C>T	GRCh37
NC_000003.10:g.134958740C>T	NCBI36
NG_013080.1:g.16074C>T
NG_013080.2:g.100209C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+197C>T MANE Select	ENSP00000385834.3:n.870+197C>T
ENST00000402696.7:c.870+197C>T	ENSP00000385834.3:n.870+197C>T
ENST00000485977.1:c.235+197C>T	ENSP00000418716.1:n.235+197C>T
NM_001063.3:c.870+197C>T	NP_001054.1:n.870+197C>T
XM_011513100.1:c.870+197C>T	XP_011511402.1:n.870+197C>T
NM_001354703.1:c.738+197C>T	NP_001341632.1:n.738+197C>T
NM_001354704.1:c.489+197C>T	NP_001341633.1:n.489+197C>T
NM_001063.4:c.870+197C>T MANE Select	NP_001054.2:n.870+197C>T
NM_001354703.2:c.738+197C>T	NP_001341632.2:n.738+197C>T
NM_001354704.2:c.489+197C>T	NP_001341633.2:n.489+197C>T