Canonical Allele Identifier: CA354610498

Gene: TF

Linked Data

• dbSNP Id: rs1452737108
• gnomAD v3: 3-133775576-G-T
• gnomAD v4: 3-133775576-G-T
• MyVariant Identifiers: chr3:g.133494420G>T (hg19) ; chr3:g.133775576G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133775576G>T , CM000665.2:g.133775576G>T	GRCh38
NC_000003.11:g.133494420G>T , CM000665.1:g.133494420G>T	GRCh37
NC_000003.10:g.134977110G>T	NCBI36
NG_013080.1:g.34444G>T
NG_013080.2:g.118579G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.1831G>T MANE Select	ENSP00000385834.3:p.Asp611Tyr
ENST00000402696.7:c.1831G>T	ENSP00000385834.3:p.Asp611Tyr
ENST00000461695.1:c.562G>T
ENST00000467842.1:n.2825G>T
NM_001063.3:c.1831G>T	NP_001054.1:p.Asp611Tyr
XM_011513100.1:c.1831G>T	XP_011511402.1:p.Asp611Tyr
NM_001354703.1:c.1699G>T	NP_001341632.1:p.Asp567Tyr
NM_001354704.1:c.1450G>T	NP_001341633.1:p.Asp484Tyr
NM_001063.4:c.1831G>T MANE Select	NP_001054.2:p.Asp611Tyr
NM_001354703.2:c.1699G>T	NP_001341632.2:p.Asp567Tyr
NM_001354704.2:c.1450G>T	NP_001341633.2:p.Asp484Tyr