Canonical Allele Identifier: CA183194664
Gene: ZFPM2 HGNC NCBI

Linked Data

dbSNP Id: rs6993770

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105569300A>T , CM000670.2:g.105569300A>T GRCh38
NC_000008.10:g.106581528A>T , CM000670.1:g.106581528A>T GRCh37
NC_000008.9:g.106650704A>T NCBI36
NG_011723.1:g.255382A>T
NG_011723.2:g.255382A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000407775.7:c.420+7819A>T MANE Select ENSP00000384179.2:n.420+7819A>T
ENST00000407775.6:c.420+7819A>T ENSP00000384179.2:n.420+7819A>T
ENST00000511341.6:n.1160+7819A>T
ENST00000517361.1:c.24+7819A>T ENSP00000428720.1:n.24+7819A>T
ENST00000520027.5:c.24+7819A>T ENSP00000428149.1:n.24+7819A>T
ENST00000520492.5:c.24+7819A>T ENSP00000430757.1:n.24+7819A>T
NM_012082.3:c.420+7819A>T NP_036214.2:n.420+7819A>T
XM_011516946.1:c.459+7819A>T XP_011515248.1:n.459+7819A>T
XM_011516947.1:c.390+7819A>T XP_011515249.1:n.390+7819A>T
XM_011516948.1:c.261+7819A>T XP_011515250.1:n.261+7819A>T
XM_011516949.1:c.459+7819A>T XP_011515251.1:n.459+7819A>T
NM_001362836.1:c.261+7819A>T NP_001349765.1:n.261+7819A>T
NM_001362837.1:c.24+7819A>T NP_001349766.1:n.24+7819A>T
XM_011516947.3:c.390+7819A>T XP_011515249.1:n.390+7819A>T
NM_012082.4:c.420+7819A>T MANE Select NP_036214.2:n.420+7819A>T
NM_001362836.2:c.261+7819A>T NP_001349765.1:n.261+7819A>T
NM_001362837.2:c.24+7819A>T NP_001349766.1:n.24+7819A>T