Canonical Allele Identifier: CA170937
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 156584
ClinVar RCV Id: RCV000144725
dbSNP Id: rs200834568

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105798763G>A , CM000670.2:g.105798763G>A GRCh38
NC_000008.10:g.106810991G>A , CM000670.1:g.106810991G>A GRCh37
NC_000008.9:g.106880167G>A NCBI36
NG_011723.1:g.484845G>A
NG_011723.2:g.484845G>A

Transcript Alleles

HGVS Amino-acid change
NM_012082.3:c.779G>A (ZFPM2) VV NP_036214.2:p.Arg260Gln
NR_125796.1:n.180-321C>T (ZFPM2-AS1)
NR_125797.1:n.191-321C>T (ZFPM2-AS1)
XM_011516946.1:c.818G>A (ZFPM2) XP_011515248.1:p.Arg273Gln
XM_011516947.1:c.749G>A (ZFPM2) XP_011515249.1:p.Arg250Gln
XM_011516948.1:c.620G>A (ZFPM2) XP_011515250.1:p.Arg207Gln
XM_011516949.1:c.611G>A (ZFPM2) XP_011515251.1:p.Arg204Gln
NM_001362836.1:c.620G>A (ZFPM2) VV NP_001349765.1:p.Arg207Gln
NM_001362837.1:c.383G>A (ZFPM2) VV NP_001349766.1:p.Arg128Gln
XM_011516947.3:c.749G>A (ZFPM2) XP_011515249.1:p.Arg250Gln
NM_012082.4:c.779G>A (ZFPM2) VV NP_036214.2:p.Arg260Gln
ENST00000407775.6:c.779G>A ENSP00000384179.2:p.Arg260Gln
ENST00000517361.1:c.383G>A ENSP00000428720.1:p.Arg128Gln
ENST00000520492.5:c.383G>A ENSP00000430757.1:p.Arg128Gln
ENST00000522296.1:n.573G>A