Canonical Allele Identifier: CA1403107706

Gene: TF

Linked Data

• dbSNP Id: rs1933861681

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133757191T>C , CM000665.2:g.133757191T>C	GRCh38
NC_000003.11:g.133476035T>C , CM000665.1:g.133476035T>C	GRCh37
NC_000003.10:g.134958725T>C	NCBI36
NG_013080.1:g.16059T>C
NG_013080.2:g.100194T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.870+182T>C MANE Select	ENSP00000385834.3:n.870+182T>C
ENST00000402696.7:c.870+182T>C	ENSP00000385834.3:n.870+182T>C
ENST00000485977.1:c.235+182T>C	ENSP00000418716.1:n.235+182T>C
NM_001063.3:c.870+182T>C	NP_001054.1:n.870+182T>C
XM_011513100.1:c.870+182T>C	XP_011511402.1:n.870+182T>C
NM_001354703.1:c.738+182T>C	NP_001341632.1:n.738+182T>C
NM_001354704.1:c.489+182T>C	NP_001341633.1:n.489+182T>C
NM_001063.4:c.870+182T>C MANE Select	NP_001054.2:n.870+182T>C
NM_001354703.2:c.738+182T>C	NP_001341632.2:n.738+182T>C
NM_001354704.2:c.489+182T>C	NP_001341633.2:n.489+182T>C