Canonical Allele Identifier: CA156092
Gene: ZNF335 HGNC NCBI

Linked Data

ClinVar Variation Id: 130802
ClinVar RCV Id: RCV000118919 RCV001512816 RCV002243772
dbSNP Id: rs11905235
ExAC: 20:44580788 G / T
gnomAD v2: 20-44580788-G-T
gnomAD v3: 20-45952149-G-T
gnomAD v4: 20-45952149-G-T
MyVariant Identifiers: chr20:g.44580788G>T (hg19) chr20:g.45952149G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45952149G>T , CM000682.2:g.45952149G>T GRCh38
NC_000020.10:g.44580788G>T , CM000682.1:g.44580788G>T GRCh37
NC_000020.9:g.44014195G>T NCBI36
NG_029772.1:g.25046C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000322927.3:c.3187C>A MANE Select ENSP00000325326.2:p.Arg1063=
ENST00000322927.2:c.3187C>A ENSP00000325326.2:p.Arg1063=
NM_022095.3:c.3187C>A NP_071378.1:p.Arg1063=
XM_005260504.3:c.3184C>A XP_005260561.1:p.Arg1062=
XM_005260506.2:c.2659C>A XP_005260563.1:p.Arg887=
XM_005260504.4:c.3184C>A XP_005260561.1:p.Arg1062=
XM_017028012.1:c.2659C>A XP_016883501.1:p.Arg887=
XR_001754372.2:n.3603C>A
XR_002958500.1:n.3583C>A
XR_002958501.1:n.3583C>A
XR_936602.3:n.3698C>A
NM_022095.4:c.3187C>A MANE Select NP_071378.1:p.Arg1063=
Search 100 bp 5'
Search 100 bp 3'