Canonical Allele Identifier: CA354604971

Gene: TF

Linked Data

• dbSNP Id: rs1390142442
• gnomAD v2: 3-133475817-G-C
• gnomAD v3: 3-133756973-G-C
• gnomAD v4: 3-133756973-G-C
• MyVariant Identifiers: chr3:g.133475817G>C (hg19) ; chr3:g.133756973G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.133756973G>C , CM000665.2:g.133756973G>C	GRCh38
NC_000003.11:g.133475817G>C , CM000665.1:g.133475817G>C	GRCh37
NC_000003.10:g.134958507G>C	NCBI36
NG_013080.1:g.15841G>C
NG_013080.2:g.99976G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402696.9:c.834G>C MANE Select	ENSP00000385834.3:p.Lys278Asn
ENST00000402696.7:c.834G>C	ENSP00000385834.3:p.Lys278Asn
ENST00000485977.1:c.199G>C	ENSP00000418716.1:p.Gly67Arg
NM_001063.3:c.834G>C	NP_001054.1:p.Lys278Asn
XM_011513100.1:c.834G>C	XP_011511402.1:p.Lys278Asn
NM_001354703.1:c.702G>C	NP_001341632.1:p.Lys234Asn
NM_001354704.1:c.453G>C	NP_001341633.1:p.Lys151Asn
NM_001063.4:c.834G>C MANE Select	NP_001054.2:p.Lys278Asn
NM_001354703.2:c.702G>C	NP_001341632.2:p.Lys234Asn
NM_001354704.2:c.453G>C	NP_001341633.2:p.Lys151Asn