Canonical Allele Identifier: CA15496513
Gene: PON2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95407680C>T , CM000669.2:g.95407680C>T GRCh38
NC_000007.13:g.95036992C>T , CM000669.1:g.95036992C>T GRCh37
NC_000007.12:g.94874928C>T NCBI36
NG_008725.1:g.32393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222572.8:c.696-612G>A MANE Select ENSP00000222572.3:n.696-612G>A
ENST00000222572.7:c.696-612G>A ENSP00000222572.3:n.696-612G>A
ENST00000433091.6:c.660-612G>A ENSP00000404622.2:n.660-612G>A
ENST00000446142.5:c.*561-612G>A ENSP00000405211.1:n.*561-612G>A
ENST00000455123.5:c.643-612G>A ENSP00000414515.1:n.643-612G>A
ENST00000483292.5:c.253-612G>A
ENST00000633192.1:c.759-612G>A ENSP00000488378.1:n.759-612G>A
ENST00000633531.1:c.696-612G>A ENSP00000488838.1:n.696-612G>A
NM_000305.2:c.696-612G>A NP_000296.2:n.696-612G>A
NM_001018161.1:c.660-612G>A NP_001018171.1:n.660-612G>A
XM_005250453.1:c.492-612G>A XP_005250510.1:n.492-612G>A
XM_005250454.1:c.486-612G>A XP_005250511.1:n.486-612G>A
XM_011516333.1:c.438-612G>A XP_011514635.1:n.438-612G>A
XM_017012357.2:c.486-612G>A XP_016867846.1:n.486-612G>A
XM_017012358.2:c.438-612G>A XP_016867847.1:n.438-612G>A
NM_000305.3:c.696-612G>A MANE Select NP_000296.2:n.696-612G>A
NM_001018161.2:c.660-612G>A NP_001018171.1:n.660-612G>A
Search 100 bp 5'
Search 100 bp 3'