Canonical Allele Identifier: CA2683810463

Gene: PON2

Linked Data

• gnomAD v4: 7-95434962-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434962C>T , CM000669.2:g.95434962C>T	GRCh38
NC_000007.13:g.95064274C>T , CM000669.1:g.95064274C>T	GRCh37
NC_000007.12:g.94902210C>T	NCBI36
NG_008725.1:g.5111G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222572.8:c.-11G>A MANE Select	ENSP00000222572.3:n.-11G>A
ENST00000222572.7:c.-11G>A	ENSP00000222572.3:n.-11G>A
ENST00000433091.6:c.-11G>A	ENSP00000404622.2:n.-11G>A
ENST00000446142.5:c.-11G>A	ENSP00000405211.1:n.-11G>A
ENST00000455123.5:c.-11G>A	ENSP00000414515.1:n.-11G>A
ENST00000469716.1:n.67G>A
ENST00000469926.5:c.-268G>A	ENSP00000488550.1:n.-268G>A
ENST00000471883.1:n.69G>A
ENST00000490778.5:c.-323G>A	ENSP00000488826.1:n.-323G>A
ENST00000493290.5:c.-344G>A	ENSP00000488822.1:n.-344G>A
ENST00000493469.5:n.2G>A
ENST00000632034.1:c.-11G>A	ENSP00000487898.1:n.-11G>A
ENST00000633192.1:c.53G>A	ENSP00000488378.1:p.Gly18Asp
ENST00000633531.1:c.-11G>A	ENSP00000488838.1:n.-11G>A
NM_000305.2:c.-11G>A	NP_000296.2:n.-11G>A
NM_001018161.1:c.-11G>A	NP_001018171.1:n.-11G>A
XM_005250453.1:c.-189G>A	XP_005250510.1:n.-189G>A
XM_005250454.1:c.-265G>A	XP_005250511.1:n.-265G>A
XM_011516333.1:c.-339G>A	XP_011514635.1:n.-339G>A
XM_017012357.2:c.-265G>A	XP_016867846.1:n.-265G>A
XM_017012358.2:c.-339G>A	XP_016867847.1:n.-339G>A
NM_000305.3:c.-11G>A MANE Select	NP_000296.2:n.-11G>A
NM_001018161.2:c.-11G>A	NP_001018171.1:n.-11G>A