Canonical Allele Identifier: CA1403124623

Gene: TF

Linked Data

• dbSNP Id: rs1559879975

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777013C>T , CM000665.2:g.133777013C>T	GRCh38
NC_000003.11:g.133495857C>T , CM000665.1:g.133495857C>T	GRCh37
NC_000003.10:g.134978547C>T	NCBI36
NG_013080.1:g.35881C>T
NG_013080.2:g.120016C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-36C>T MANE Select	ENSP00000385834.3:n.1873-36C>T
ENST00000402696.7:c.1873-36C>T	ENSP00000385834.3:n.1873-36C>T
ENST00000461695.1:c.604-36C>T
ENST00000467842.1:n.2867-36C>T
NM_001063.3:c.1873-36C>T	NP_001054.1:n.1873-36C>T
XM_011513100.1:c.1873-36C>T	XP_011511402.1:n.1873-36C>T
NM_001354703.1:c.1741-36C>T	NP_001341632.1:n.1741-36C>T
NM_001354704.1:c.1492-36C>T	NP_001341633.1:n.1492-36C>T
NM_001063.4:c.1873-36C>T MANE Select	NP_001054.2:n.1873-36C>T
NM_001354703.2:c.1741-36C>T	NP_001341632.2:n.1741-36C>T
NM_001354704.2:c.1492-36C>T	NP_001341633.2:n.1492-36C>T