Canonical Allele Identifier: CA354604982

Gene: TF

Linked Data

• dbSNP Id: rs542696572
• gnomAD v2: 3-133475821-G-T
• gnomAD v4: 3-133756977-G-T
• MyVariant Identifiers: chr3:g.133475821G>T (hg19) ; chr3:g.133756977G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756977G>T , CM000665.2:g.133756977G>T	GRCh38
NC_000003.11:g.133475821G>T , CM000665.1:g.133475821G>T	GRCh37
NC_000003.10:g.134958511G>T	NCBI36
NG_013080.1:g.15845G>T
NG_013080.2:g.99980G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.838G>T MANE Select	ENSP00000385834.3:p.Asp280Tyr
ENST00000402696.7:c.838G>T	ENSP00000385834.3:p.Asp280Tyr
ENST00000485977.1:c.203G>T	ENSP00000418716.1:p.Gly68Val
NM_001063.3:c.838G>T	NP_001054.1:p.Asp280Tyr
XM_011513100.1:c.838G>T	XP_011511402.1:p.Asp280Tyr
NM_001354703.1:c.706G>T	NP_001341632.1:p.Asp236Tyr
NM_001354704.1:c.457G>T	NP_001341633.1:p.Asp153Tyr
NM_001063.4:c.838G>T MANE Select	NP_001054.2:p.Asp280Tyr
NM_001354703.2:c.706G>T	NP_001341632.2:p.Asp236Tyr
NM_001354704.2:c.457G>T	NP_001341633.2:p.Asp153Tyr