Canonical Allele Identifier: CA2683810460

Gene: PON2

Linked Data

• gnomAD v4: 7-95434961-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434961G>C , CM000669.2:g.95434961G>C	GRCh38
NC_000007.13:g.95064273G>C , CM000669.1:g.95064273G>C	GRCh37
NC_000007.12:g.94902209G>C	NCBI36
NG_008725.1:g.5112C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222572.8:c.-10C>G MANE Select	ENSP00000222572.3:n.-10C>G
ENST00000222572.7:c.-10C>G	ENSP00000222572.3:n.-10C>G
ENST00000433091.6:c.-10C>G	ENSP00000404622.2:n.-10C>G
ENST00000446142.5:c.-10C>G	ENSP00000405211.1:n.-10C>G
ENST00000455123.5:c.-10C>G	ENSP00000414515.1:n.-10C>G
ENST00000469716.1:n.68C>G
ENST00000469926.5:c.-267C>G	ENSP00000488550.1:n.-267C>G
ENST00000471883.1:n.70C>G
ENST00000490778.5:c.-322C>G	ENSP00000488826.1:n.-322C>G
ENST00000493290.5:c.-343C>G	ENSP00000488822.1:n.-343C>G
ENST00000493469.5:n.3C>G
ENST00000632034.1:c.-10C>G	ENSP00000487898.1:n.-10C>G
ENST00000633192.1:c.54C>G	ENSP00000488378.1:p.Gly18=
ENST00000633531.1:c.-10C>G	ENSP00000488838.1:n.-10C>G
NM_000305.2:c.-10C>G	NP_000296.2:n.-10C>G
NM_001018161.1:c.-10C>G	NP_001018171.1:n.-10C>G
XM_005250453.1:c.-188C>G	XP_005250510.1:n.-188C>G
XM_005250454.1:c.-264C>G	XP_005250511.1:n.-264C>G
XM_011516333.1:c.-338C>G	XP_011514635.1:n.-338C>G
XM_017012357.2:c.-264C>G	XP_016867846.1:n.-264C>G
XM_017012358.2:c.-338C>G	XP_016867847.1:n.-338C>G
NM_000305.3:c.-10C>G MANE Select	NP_000296.2:n.-10C>G
NM_001018161.2:c.-10C>G	NP_001018171.1:n.-10C>G