Canonical Allele Identifier: CA118611
Gene: PON2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95405463G>C , CM000669.2:g.95405463G>C GRCh38
NC_000007.13:g.95034775G>C , CM000669.1:g.95034775G>C GRCh37
NC_000007.12:g.94872711G>C NCBI36
NG_008725.1:g.34610C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222572.8:c.932C>G MANE Select ENSP00000222572.3:p.Ser311Cys
ENST00000222572.7:c.932C>G ENSP00000222572.3:p.Ser311Cys
ENST00000433091.6:c.896C>G ENSP00000404622.2:p.Ser299Cys
ENST00000446142.5:c.*797C>G ENSP00000405211.1:n.*797C>G
ENST00000455123.5:c.*219C>G ENSP00000414515.1:n.*219C>G
ENST00000483292.5:c.514C>G
ENST00000633192.1:c.995C>G ENSP00000488378.1:p.Ser332Cys
ENST00000633531.1:c.932C>G ENSP00000488838.1:p.Ser311Cys
NM_000305.2:c.932C>G NP_000296.2:p.Ser311Cys
NM_001018161.1:c.896C>G NP_001018171.1:p.Ser299Cys
XM_005250453.1:c.728C>G XP_005250510.1:p.Ser243Cys
XM_005250454.1:c.722C>G XP_005250511.1:p.Ser241Cys
XM_011516333.1:c.674C>G XP_011514635.1:p.Ser225Cys
XM_017012357.2:c.722C>G XP_016867846.1:p.Ser241Cys
XM_017012358.2:c.674C>G XP_016867847.1:p.Ser225Cys
NM_000305.3:c.932C>G MANE Select NP_000296.2:p.Ser311Cys
NM_001018161.2:c.896C>G NP_001018171.1:p.Ser299Cys