Canonical Allele Identifier: CA2683810472

Gene: PON2

Linked Data

• gnomAD v4: 7-95434968-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434968G>A , CM000669.2:g.95434968G>A	GRCh38
NC_000007.13:g.95064280G>A , CM000669.1:g.95064280G>A	GRCh37
NC_000007.12:g.94902216G>A	NCBI36
NG_008725.1:g.5105C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222572.8:c.-17C>T MANE Select	ENSP00000222572.3:n.-17C>T
ENST00000222572.7:c.-17C>T	ENSP00000222572.3:n.-17C>T
ENST00000433091.6:c.-17C>T	ENSP00000404622.2:n.-17C>T
ENST00000446142.5:c.-17C>T	ENSP00000405211.1:n.-17C>T
ENST00000455123.5:c.-17C>T	ENSP00000414515.1:n.-17C>T
ENST00000469716.1:n.61C>T
ENST00000469926.5:c.-274C>T	ENSP00000488550.1:n.-274C>T
ENST00000471883.1:n.63C>T
ENST00000490778.5:c.-329C>T	ENSP00000488826.1:n.-329C>T
ENST00000493290.5:c.-350C>T	ENSP00000488822.1:n.-350C>T
ENST00000632034.1:c.-17C>T	ENSP00000487898.1:n.-17C>T
ENST00000633192.1:c.47C>T	ENSP00000488378.1:p.Ala16Val
ENST00000633531.1:c.-17C>T	ENSP00000488838.1:n.-17C>T
NM_000305.2:c.-17C>T	NP_000296.2:n.-17C>T
NM_001018161.1:c.-17C>T	NP_001018171.1:n.-17C>T
XM_005250453.1:c.-195C>T	XP_005250510.1:n.-195C>T
XM_005250454.1:c.-271C>T	XP_005250511.1:n.-271C>T
XM_011516333.1:c.-345C>T	XP_011514635.1:n.-345C>T
XM_017012357.2:c.-271C>T	XP_016867846.1:n.-271C>T
XM_017012358.2:c.-345C>T	XP_016867847.1:n.-345C>T
NM_000305.3:c.-17C>T MANE Select	NP_000296.2:n.-17C>T
NM_001018161.2:c.-17C>T	NP_001018171.1:n.-17C>T