Canonical Allele Identifier: CA371951166
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1814021362

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801670C>T , CM000670.2:g.105801670C>T GRCh38
NC_000008.10:g.106813898C>T , CM000670.1:g.106813898C>T GRCh37
NC_000008.9:g.106883074C>T NCBI36
NG_011723.1:g.487752C>T
NG_011723.2:g.487752C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000407775.7:c.1588C>T (ZFPM2) MANE Select ENSP00000384179.2:p.His530Tyr
ENST00000407775.6:c.1588C>T (ZFPM2) ENSP00000384179.2:p.His530Tyr
ENST00000517361.1:c.1192C>T (ZFPM2) ENSP00000428720.1:p.His398Tyr
ENST00000520492.5:c.1192C>T (ZFPM2) ENSP00000430757.1:p.His398Tyr
ENST00000522296.1:n.1382C>T (ZFPM2)
NM_012082.3:c.1588C>T (ZFPM2) NP_036214.2:p.His530Tyr
NR_125796.1:n.180-3228G>A (ZFPM2-AS1)
NR_125797.1:n.191-3228G>A (ZFPM2-AS1)
XM_011516946.1:c.1627C>T (ZFPM2) XP_011515248.1:p.His543Tyr
XM_011516947.1:c.1558C>T (ZFPM2) XP_011515249.1:p.His520Tyr
XM_011516948.1:c.1429C>T (ZFPM2) XP_011515250.1:p.His477Tyr
XM_011516949.1:c.1420C>T (ZFPM2) XP_011515251.1:p.His474Tyr
NM_001362836.1:c.1429C>T (ZFPM2) NP_001349765.1:p.His477Tyr
NM_001362837.1:c.1192C>T (ZFPM2) NP_001349766.1:p.His398Tyr
XM_011516947.3:c.1558C>T (ZFPM2) XP_011515249.1:p.His520Tyr
NM_012082.4:c.1588C>T (ZFPM2) MANE Select NP_036214.2:p.His530Tyr
NM_001362836.2:c.1429C>T (ZFPM2) NP_001349765.1:p.His477Tyr
NM_001362837.2:c.1192C>T (ZFPM2) NP_001349766.1:p.His398Tyr