Canonical Allele Identifier: CA1403130543

Gene: TF

Linked Data

• dbSNP Id: rs1934355062
• gnomAD v4: 3-133775194-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775194G>C , CM000665.2:g.133775194G>C	GRCh38
NC_000003.11:g.133494038G>C , CM000665.1:g.133494038G>C	GRCh37
NC_000003.10:g.134976728G>C	NCBI36
NG_013080.1:g.34062G>C
NG_013080.2:g.118197G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1688-239G>C MANE Select	ENSP00000385834.3:n.1688-239G>C
ENST00000402696.7:c.1688-239G>C	ENSP00000385834.3:n.1688-239G>C
ENST00000461695.1:c.419-239G>C
ENST00000467842.1:n.2443G>C
NM_001063.3:c.1688-239G>C	NP_001054.1:n.1688-239G>C
XM_011513100.1:c.1688-239G>C	XP_011511402.1:n.1688-239G>C
NM_001354703.1:c.1556-239G>C	NP_001341632.1:n.1556-239G>C
NM_001354704.1:c.1307-239G>C	NP_001341633.1:n.1307-239G>C
NM_001063.4:c.1688-239G>C MANE Select	NP_001054.2:n.1688-239G>C
NM_001354703.2:c.1556-239G>C	NP_001341632.2:n.1556-239G>C
NM_001354704.2:c.1307-239G>C	NP_001341633.2:n.1307-239G>C