Canonical Allele Identifier: CA2625300

Gene: TF

Linked Data

• dbSNP Id: rs781390866
• ExAC: 3:133485227 G / A
• gnomAD v2: 3-133485227-G-A
• gnomAD v3: 3-133766383-G-A
• gnomAD v4: 3-133766383-G-A
• MyVariant Identifiers: chr3:g.133485227G>A (hg19) ; chr3:g.133766383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766383G>A , CM000665.2:g.133766383G>A	GRCh38
NC_000003.11:g.133485227G>A , CM000665.1:g.133485227G>A	GRCh37
NC_000003.10:g.134967917G>A	NCBI36
NG_013080.1:g.25251G>A
NG_013080.2:g.109386G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1436G>A MANE Select	ENSP00000385834.3:p.Trp479Ter
ENST00000402696.7:c.1436G>A	ENSP00000385834.3:p.Trp479Ter
ENST00000461695.1:c.106G>A
NM_001063.3:c.1436G>A	NP_001054.1:p.Trp479Ter
XM_011513100.1:c.1436G>A	XP_011511402.1:p.Trp479Ter
NM_001354703.1:c.1304G>A	NP_001341632.1:p.Trp435Ter
NM_001354704.1:c.1055G>A	NP_001341633.1:p.Trp352Ter
NM_001063.4:c.1436G>A MANE Select	NP_001054.2:p.Trp479Ter
NM_001354703.2:c.1304G>A	NP_001341632.2:p.Trp435Ter
NM_001354704.2:c.1055G>A	NP_001341633.2:p.Trp352Ter