Canonical Allele Identifier: CA162954013

Gene: PON2

Linked Data

• dbSNP Id: rs1024414526
• gnomAD v4: 7-95434964-G-C
• MyVariant Identifiers: chr7:g.95064276G>C (hg19) ; chr7:g.95434964G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434964G>C , CM000669.2:g.95434964G>C	GRCh38
NC_000007.13:g.95064276G>C , CM000669.1:g.95064276G>C	GRCh37
NC_000007.12:g.94902212G>C	NCBI36
NG_008725.1:g.5109C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222572.8:c.-13C>G MANE Select	ENSP00000222572.3:n.-13C>G
ENST00000222572.7:c.-13C>G	ENSP00000222572.3:n.-13C>G
ENST00000433091.6:c.-13C>G	ENSP00000404622.2:n.-13C>G
ENST00000446142.5:c.-13C>G	ENSP00000405211.1:n.-13C>G
ENST00000455123.5:c.-13C>G	ENSP00000414515.1:n.-13C>G
ENST00000469716.1:n.65C>G
ENST00000469926.5:c.-270C>G	ENSP00000488550.1:n.-270C>G
ENST00000471883.1:n.67C>G
ENST00000490778.5:c.-325C>G	ENSP00000488826.1:n.-325C>G
ENST00000493290.5:c.-346C>G	ENSP00000488822.1:n.-346C>G
ENST00000632034.1:c.-13C>G	ENSP00000487898.1:n.-13C>G
ENST00000633192.1:c.51C>G	ENSP00000488378.1:p.Pro17=
ENST00000633531.1:c.-13C>G	ENSP00000488838.1:n.-13C>G
NM_000305.2:c.-13C>G	NP_000296.2:n.-13C>G
NM_001018161.1:c.-13C>G	NP_001018171.1:n.-13C>G
XM_005250453.1:c.-191C>G	XP_005250510.1:n.-191C>G
XM_005250454.1:c.-267C>G	XP_005250511.1:n.-267C>G
XM_011516333.1:c.-341C>G	XP_011514635.1:n.-341C>G
XM_017012357.2:c.-267C>G	XP_016867846.1:n.-267C>G
XM_017012358.2:c.-341C>G	XP_016867847.1:n.-341C>G
NM_000305.3:c.-13C>G MANE Select	NP_000296.2:n.-13C>G
NM_001018161.2:c.-13C>G	NP_001018171.1:n.-13C>G