Canonical Allele Identifier: CA354608721

Gene: TF

Linked Data

• dbSNP Id: rs121918679
• gnomAD v4: 3-133766376-G-T
• MyVariant Identifiers: chr3:g.133485220G>T (hg19) ; chr3:g.133766376G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133766376G>T , CM000665.2:g.133766376G>T	GRCh38
NC_000003.11:g.133485220G>T , CM000665.1:g.133485220G>T	GRCh37
NC_000003.10:g.134967910G>T	NCBI36
NG_013080.1:g.25244G>T
NG_013080.2:g.109379G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402696.9:c.1429G>T MANE Select	ENSP00000385834.3:p.Ala477Ser
ENST00000402696.7:c.1429G>T	ENSP00000385834.3:p.Ala477Ser
ENST00000461695.1:c.99G>T
NM_001063.3:c.1429G>T	NP_001054.1:p.Ala477Ser
XM_011513100.1:c.1429G>T	XP_011511402.1:p.Ala477Ser
NM_001354703.1:c.1297G>T	NP_001341632.1:p.Ala433Ser
NM_001354704.1:c.1048G>T	NP_001341633.1:p.Ala350Ser
NM_001063.4:c.1429G>T MANE Select	NP_001054.2:p.Ala477Ser
NM_001354703.2:c.1297G>T	NP_001341632.2:p.Ala433Ser
NM_001354704.2:c.1048G>T	NP_001341633.2:p.Ala350Ser