Canonical Allele Identifier: CA354608772

Gene: TF

Linked Data

• gnomAD v4: 3-133766398-G-C
• MyVariant Identifiers: chr3:g.133485242G>C (hg19) ; chr3:g.133766398G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766398G>C , CM000665.2:g.133766398G>C	GRCh38
NC_000003.11:g.133485242G>C , CM000665.1:g.133485242G>C	GRCh37
NC_000003.10:g.134967932G>C	NCBI36
NG_013080.1:g.25266G>C
NG_013080.2:g.109401G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1451G>C MANE Select	ENSP00000385834.3:p.Gly484Ala
ENST00000402696.7:c.1451G>C	ENSP00000385834.3:p.Gly484Ala
ENST00000461695.1:c.121G>C
NM_001063.3:c.1451G>C	NP_001054.1:p.Gly484Ala
XM_011513100.1:c.1451G>C	XP_011511402.1:p.Gly484Ala
NM_001354703.1:c.1319G>C	NP_001341632.1:p.Gly440Ala
NM_001354704.1:c.1070G>C	NP_001341633.1:p.Gly357Ala
NM_001063.4:c.1451G>C MANE Select	NP_001054.2:p.Gly484Ala
NM_001354703.2:c.1319G>C	NP_001341632.2:p.Gly440Ala
NM_001354704.2:c.1070G>C	NP_001341633.2:p.Gly357Ala