Canonical Allele Identifier: CA354605013

Gene: TF

Linked Data

• dbSNP Id: rs1255911148
• gnomAD v3: 3-133756990-A-G
• gnomAD v4: 3-133756990-A-G
• MyVariant Identifiers: chr3:g.133475834A>G (hg19) ; chr3:g.133756990A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756990A>G , CM000665.2:g.133756990A>G	GRCh38
NC_000003.11:g.133475834A>G , CM000665.1:g.133475834A>G	GRCh37
NC_000003.10:g.134958524A>G	NCBI36
NG_013080.1:g.15858A>G
NG_013080.2:g.99993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.851A>G MANE Select	ENSP00000385834.3:p.Glu284Gly
ENST00000402696.7:c.851A>G	ENSP00000385834.3:p.Glu284Gly
ENST00000485977.1:c.216A>G	ENSP00000418716.1:p.Gly72=
NM_001063.3:c.851A>G	NP_001054.1:p.Glu284Gly
XM_011513100.1:c.851A>G	XP_011511402.1:p.Glu284Gly
NM_001354703.1:c.719A>G	NP_001341632.1:p.Glu240Gly
NM_001354704.1:c.470A>G	NP_001341633.1:p.Glu157Gly
NM_001063.4:c.851A>G MANE Select	NP_001054.2:p.Glu284Gly
NM_001354703.2:c.719A>G	NP_001341632.2:p.Glu240Gly
NM_001354704.2:c.470A>G	NP_001341633.2:p.Glu157Gly