Canonical Allele Identifier: CA1727228062
Gene: PON2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95434956C= , CM000669.2:g.95434956C= GRCh38
NC_000007.13:g.95064268C= , CM000669.1:g.95064268C= GRCh37
NC_000007.12:g.94902204C= NCBI36
NG_008725.1:g.5117G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222572.8:c.-5G= MANE Select ENSP00000222572.3:n.-5G=
ENST00000222572.7:c.-5G= ENSP00000222572.3:n.-5G=
ENST00000433091.6:c.-5G= ENSP00000404622.2:n.-5G=
ENST00000446142.5:c.-5G= ENSP00000405211.1:n.-5G=
ENST00000455123.5:c.-5G= ENSP00000414515.1:n.-5G=
ENST00000469716.1:n.73G=
ENST00000469926.5:c.-262G= ENSP00000488550.1:n.-262G=
ENST00000471883.1:n.75G=
ENST00000490778.5:c.-317G= ENSP00000488826.1:n.-317G=
ENST00000493290.5:c.-338G= ENSP00000488822.1:n.-338G=
ENST00000493469.5:n.8G=
ENST00000632034.1:c.-5G= ENSP00000487898.1:n.-5G=
ENST00000633192.1:c.59G= ENSP00000488378.1:p.Arg20=
ENST00000633531.1:c.-5G= ENSP00000488838.1:n.-5G=
NM_000305.2:c.-5G= NP_000296.2:n.-5G=
NM_001018161.1:c.-5G= NP_001018171.1:n.-5G=
XM_005250453.1:c.-183G= XP_005250510.1:n.-183G=
XM_005250454.1:c.-259G= XP_005250511.1:n.-259G=
XM_011516333.1:c.-333G= XP_011514635.1:n.-333G=
XM_017012357.2:c.-259G= XP_016867846.1:n.-259G=
XM_017012358.2:c.-333G= XP_016867847.1:n.-333G=
NM_000305.3:c.-5G= MANE Select NP_000296.2:n.-5G=
NM_001018161.2:c.-5G= NP_001018171.1:n.-5G=