Canonical Allele Identifier: CA409250094

Gene: ZNF335

Linked Data

• ClinVar Variation Id: 445926
• ClinVar RCV Id: RCV000514674
• dbSNP Id: rs1234838549
• gnomAD v3: 20-45963651-C-T
• gnomAD v4: 20-45963651-C-T
• MyVariant Identifiers: chr20:g.44592290C>T (hg19) ; chr20:g.45963651C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45963651C>T , CM000682.2:g.45963651C>T	GRCh38
NC_000020.10:g.44592290C>T , CM000682.1:g.44592290C>T	GRCh37
NC_000020.9:g.44025697C>T	NCBI36
NG_029772.1:g.13544G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322927.3:c.1356-1G>A MANE Select	ENSP00000325326.2:n.1356-1G>A
ENST00000322927.2:c.1356-1G>A	ENSP00000325326.2:n.1356-1G>A
ENST00000475002.1:n.866G>A
NM_022095.3:c.1356-1G>A	NP_071378.1:n.1356-1G>A
XM_005260504.3:c.1353-1G>A	XP_005260561.1:n.1353-1G>A
XM_005260506.2:c.828-1G>A	XP_005260563.1:n.828-1G>A
XM_011528979.1:c.1356-1G>A	XP_011527281.1:n.1356-1G>A
XR_936602.1:n.1867-1G>A
XR_936603.1:n.1868-1G>A
XR_936604.1:n.1868-1G>A
XM_005260504.4:c.1353-1G>A	XP_005260561.1:n.1353-1G>A
XM_011528979.3:c.1356-1G>A	XP_011527281.1:n.1356-1G>A
XM_017028012.1:c.828-1G>A	XP_016883501.1:n.828-1G>A
XR_001754372.2:n.1847-1G>A
XR_002958500.1:n.1847-1G>A
XR_002958501.1:n.1847-1G>A
XR_936602.3:n.1847-1G>A
XR_936604.3:n.1847-1G>A
NM_022095.4:c.1356-1G>A MANE Select	NP_071378.1:n.1356-1G>A