Canonical Allele Identifier: CA2625438

Gene: TF

Linked Data

• dbSNP Id: rs770899237
• ExAC: 3:133495864 T / C
• gnomAD v2: 3-133495864-T-C
• gnomAD v4: 3-133777020-T-C
• MyVariant Identifiers: chr3:g.133495864T>C (hg19) ; chr3:g.133777020T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133777020T>C , CM000665.2:g.133777020T>C	GRCh38
NC_000003.11:g.133495864T>C , CM000665.1:g.133495864T>C	GRCh37
NC_000003.10:g.134978554T>C	NCBI36
NG_013080.1:g.35888T>C
NG_013080.2:g.120023T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1873-29T>C MANE Select	ENSP00000385834.3:n.1873-29T>C
ENST00000402696.7:c.1873-29T>C	ENSP00000385834.3:n.1873-29T>C
ENST00000461695.1:c.604-29T>C
ENST00000467842.1:n.2867-29T>C
NM_001063.3:c.1873-29T>C	NP_001054.1:n.1873-29T>C
XM_011513100.1:c.1873-29T>C	XP_011511402.1:n.1873-29T>C
NM_001354703.1:c.1741-29T>C	NP_001341632.1:n.1741-29T>C
NM_001354704.1:c.1492-29T>C	NP_001341633.1:n.1492-29T>C
NM_001063.4:c.1873-29T>C MANE Select	NP_001054.2:n.1873-29T>C
NM_001354703.2:c.1741-29T>C	NP_001341632.2:n.1741-29T>C
NM_001354704.2:c.1492-29T>C	NP_001341633.2:n.1492-29T>C