Canonical Allele Identifier: CA156103

Gene: ZNF335

Linked Data

• ClinVar Variation Id: 130810
• ClinVar RCV Id: RCV000118927 ; RCV001519401 ; RCV002243779
• dbSNP Id: rs6032606
• ExAC: 20:44596207 C / G
• gnomAD v2: 20-44596207-C-G
• gnomAD v3: 20-45967568-C-G
• gnomAD v4: 20-45967568-C-G
• MyVariant Identifiers: chr20:g.44596207C>G (hg19) ; chr20:g.45967568C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45967568C>G , CM000682.2:g.45967568C>G	GRCh38
NC_000020.10:g.44596207C>G , CM000682.1:g.44596207C>G	GRCh37
NC_000020.9:g.44029614C>G	NCBI36
NG_029772.1:g.9627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322927.3:c.881G>C MANE Select	ENSP00000325326.2:p.Ser294Thr
ENST00000322927.2:c.881G>C	ENSP00000325326.2:p.Ser294Thr
ENST00000476822.1:n.1214G>C
ENST00000494955.1:n.1192G>C
NM_022095.3:c.881G>C	NP_071378.1:p.Ser294Thr
XM_005260504.3:c.878G>C	XP_005260561.1:p.Ser293Thr
XM_005260506.2:c.353G>C	XP_005260563.1:p.Ser118Thr
XM_011528979.1:c.881G>C	XP_011527281.1:p.Ser294Thr
XR_936602.1:n.1392G>C
XR_936603.1:n.1393G>C
XR_936604.1:n.1393G>C
XM_005260504.4:c.878G>C	XP_005260561.1:p.Ser293Thr
XM_011528979.3:c.881G>C	XP_011527281.1:p.Ser294Thr
XM_017028012.1:c.353G>C	XP_016883501.1:p.Ser118Thr
XR_001754372.2:n.1372G>C
XR_002958500.1:n.1372G>C
XR_002958501.1:n.1372G>C
XR_936602.3:n.1372G>C
XR_936604.3:n.1372G>C
NM_022095.4:c.881G>C MANE Select	NP_071378.1:p.Ser294Thr