Canonical Allele Identifier: CA9885839

Gene: ZNF335

Linked Data

• ClinVar Variation Id: 446071
• ClinVar RCV Id: RCV000514060 ; RCV002244985
• dbSNP Id: rs112458662
• ExAC: 20:44594258 A / G
• gnomAD v2: 20-44594258-A-G
• gnomAD v3: 20-45965619-A-G
• gnomAD v4: 20-45965619-A-G
• MyVariant Identifiers: chr20:g.44594258A>G (hg19) ; chr20:g.45965619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45965619A>G , CM000682.2:g.45965619A>G	GRCh38
NC_000020.10:g.44594258A>G , CM000682.1:g.44594258A>G	GRCh37
NC_000020.9:g.44027665A>G	NCBI36
NG_029772.1:g.11576T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322927.3:c.1102+9T>C MANE Select	ENSP00000325326.2:n.1102+9T>C
ENST00000322927.2:c.1102+9T>C	ENSP00000325326.2:n.1102+9T>C
NM_022095.3:c.1102+9T>C	NP_071378.1:n.1102+9T>C
XM_005260504.3:c.1099+9T>C	XP_005260561.1:n.1099+9T>C
XM_005260506.2:c.574+9T>C	XP_005260563.1:n.574+9T>C
XM_011528979.1:c.1102+9T>C	XP_011527281.1:n.1102+9T>C
XR_936602.1:n.1613+9T>C
XR_936603.1:n.1614+9T>C
XR_936604.1:n.1614+9T>C
XM_005260504.4:c.1099+9T>C	XP_005260561.1:n.1099+9T>C
XM_011528979.3:c.1102+9T>C	XP_011527281.1:n.1102+9T>C
XM_017028012.1:c.574+9T>C	XP_016883501.1:n.574+9T>C
XR_001754372.2:n.1593+9T>C
XR_002958500.1:n.1593+9T>C
XR_002958501.1:n.1593+9T>C
XR_936602.3:n.1593+9T>C
XR_936604.3:n.1593+9T>C
NM_022095.4:c.1102+9T>C MANE Select	NP_071378.1:n.1102+9T>C