Canonical Allele Identifier: CA9884741

Gene: ZNF335

Linked Data

• ClinVar Variation Id: 453188
• ClinVar RCV Id: RCV000520219 ; RCV000709924
• dbSNP Id: rs200635860
• ExAC: 20:44577623 T / C
• gnomAD v2: 20-44577623-T-C
• gnomAD v3: 20-45948984-T-C
• gnomAD v4: 20-45948984-T-C
• MyVariant Identifiers: chr20:g.44577623T>C (hg19) ; chr20:g.45948984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45948984T>C , CM000682.2:g.45948984T>C	GRCh38
NC_000020.10:g.44577623T>C , CM000682.1:g.44577623T>C	GRCh37
NC_000020.9:g.44011030T>C	NCBI36
NG_029772.1:g.28211A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322927.3:c.3998A>G MANE Select	ENSP00000325326.2:p.Glu1333Gly
ENST00000322927.2:c.3998A>G	ENSP00000325326.2:p.Glu1333Gly
NM_022095.3:c.3998A>G	NP_071378.1:p.Glu1333Gly
XM_005260504.3:c.3995A>G	XP_005260561.1:p.Glu1332Gly
XM_005260506.2:c.3470A>G	XP_005260563.1:p.Glu1157Gly
XM_005260504.4:c.3995A>G	XP_005260561.1:p.Glu1332Gly
XM_017028012.1:c.3470A>G	XP_016883501.1:p.Glu1157Gly
XR_002958500.1:n.5945A>G
XR_002958501.1:n.4625A>G
XR_936602.3:n.4509A>G
NM_022095.4:c.3998A>G MANE Select	NP_071378.1:p.Glu1333Gly