Canonical Allele Identifier: CA354610085

Gene: TF

Linked Data

• dbSNP Id: rs1225787241
• gnomAD v2: 3-133494285-C-T
• gnomAD v4: 3-133775441-C-T
• MyVariant Identifiers: chr3:g.133494285C>T (hg19) ; chr3:g.133775441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775441C>T , CM000665.2:g.133775441C>T	GRCh38
NC_000003.11:g.133494285C>T , CM000665.1:g.133494285C>T	GRCh37
NC_000003.10:g.134976975C>T	NCBI36
NG_013080.1:g.34309C>T
NG_013080.2:g.118444C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1696C>T MANE Select	ENSP00000385834.3:p.Pro566Ser
ENST00000402696.7:c.1696C>T	ENSP00000385834.3:p.Pro566Ser
ENST00000461695.1:c.427C>T
ENST00000467842.1:n.2690C>T
NM_001063.3:c.1696C>T	NP_001054.1:p.Pro566Ser
XM_011513100.1:c.1696C>T	XP_011511402.1:p.Pro566Ser
NM_001354703.1:c.1564C>T	NP_001341632.1:p.Pro522Ser
NM_001354704.1:c.1315C>T	NP_001341633.1:p.Pro439Ser
NM_001063.4:c.1696C>T MANE Select	NP_001054.2:p.Pro566Ser
NM_001354703.2:c.1564C>T	NP_001341632.2:p.Pro522Ser
NM_001354704.2:c.1315C>T	NP_001341633.2:p.Pro439Ser