Canonical Allele Identifier: CA2683810469

Gene: PON2

Linked Data

• gnomAD v4: 7-95434966-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434966G>T , CM000669.2:g.95434966G>T	GRCh38
NC_000007.13:g.95064278G>T , CM000669.1:g.95064278G>T	GRCh37
NC_000007.12:g.94902214G>T	NCBI36
NG_008725.1:g.5107C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222572.8:c.-15C>A MANE Select	ENSP00000222572.3:n.-15C>A
ENST00000222572.7:c.-15C>A	ENSP00000222572.3:n.-15C>A
ENST00000433091.6:c.-15C>A	ENSP00000404622.2:n.-15C>A
ENST00000446142.5:c.-15C>A	ENSP00000405211.1:n.-15C>A
ENST00000455123.5:c.-15C>A	ENSP00000414515.1:n.-15C>A
ENST00000469716.1:n.63C>A
ENST00000469926.5:c.-272C>A	ENSP00000488550.1:n.-272C>A
ENST00000471883.1:n.65C>A
ENST00000490778.5:c.-327C>A	ENSP00000488826.1:n.-327C>A
ENST00000493290.5:c.-348C>A	ENSP00000488822.1:n.-348C>A
ENST00000632034.1:c.-15C>A	ENSP00000487898.1:n.-15C>A
ENST00000633192.1:c.49C>A	ENSP00000488378.1:p.Pro17Thr
ENST00000633531.1:c.-15C>A	ENSP00000488838.1:n.-15C>A
NM_000305.2:c.-15C>A	NP_000296.2:n.-15C>A
NM_001018161.1:c.-15C>A	NP_001018171.1:n.-15C>A
XM_005250453.1:c.-193C>A	XP_005250510.1:n.-193C>A
XM_005250454.1:c.-269C>A	XP_005250511.1:n.-269C>A
XM_011516333.1:c.-343C>A	XP_011514635.1:n.-343C>A
XM_017012357.2:c.-269C>A	XP_016867846.1:n.-269C>A
XM_017012358.2:c.-343C>A	XP_016867847.1:n.-343C>A
NM_000305.3:c.-15C>A MANE Select	NP_000296.2:n.-15C>A
NM_001018161.2:c.-15C>A	NP_001018171.1:n.-15C>A