Canonical Allele Identifier: CA462650068
Gene: ZFPM2 HGNC NCBI
ZFPM2-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.106814179A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.105801951A>T , CM000670.2:g.105801951A>T GRCh38
NC_000008.10:g.106814179A>T , CM000670.1:g.106814179A>T GRCh37
NC_000008.9:g.106883355A>T NCBI36
NG_011723.1:g.488033A>T
NG_011723.2:g.488033A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000407775.7:c.1869A>T (ZFPM2) MANE Select ENSP00000384179.2:p.Thr623=
ENST00000407775.6:c.1869A>T (ZFPM2) ENSP00000384179.2:p.Thr623=
ENST00000517361.1:c.1473A>T (ZFPM2) ENSP00000428720.1:p.Thr491=
ENST00000520492.5:c.1473A>T (ZFPM2) ENSP00000430757.1:p.Thr491=
ENST00000522296.1:n.1663A>T (ZFPM2)
NM_012082.3:c.1869A>T (ZFPM2) NP_036214.2:p.Thr623=
NR_125796.1:n.180-3509T>A (ZFPM2-AS1)
NR_125797.1:n.191-3509T>A (ZFPM2-AS1)
XM_011516946.1:c.1908A>T (ZFPM2) XP_011515248.1:p.Thr636=
XM_011516947.1:c.1839A>T (ZFPM2) XP_011515249.1:p.Thr613=
XM_011516948.1:c.1710A>T (ZFPM2) XP_011515250.1:p.Thr570=
XM_011516949.1:c.1701A>T (ZFPM2) XP_011515251.1:p.Thr567=
NM_001362836.1:c.1710A>T (ZFPM2) NP_001349765.1:p.Thr570=
NM_001362837.1:c.1473A>T (ZFPM2) NP_001349766.1:p.Thr491=
XM_011516947.3:c.1839A>T (ZFPM2) XP_011515249.1:p.Thr613=
NM_012082.4:c.1869A>T (ZFPM2) MANE Select NP_036214.2:p.Thr623=
NM_001362836.2:c.1710A>T (ZFPM2) NP_001349765.1:p.Thr570=
NM_001362837.2:c.1473A>T (ZFPM2) NP_001349766.1:p.Thr491=