Canonical Allele Identifier: CA2683810464

Gene: PON2

Linked Data

• gnomAD v4: 7-95434963-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434963C>G , CM000669.2:g.95434963C>G	GRCh38
NC_000007.13:g.95064275C>G , CM000669.1:g.95064275C>G	GRCh37
NC_000007.12:g.94902211C>G	NCBI36
NG_008725.1:g.5110G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222572.8:c.-12G>C MANE Select	ENSP00000222572.3:n.-12G>C
ENST00000222572.7:c.-12G>C	ENSP00000222572.3:n.-12G>C
ENST00000433091.6:c.-12G>C	ENSP00000404622.2:n.-12G>C
ENST00000446142.5:c.-12G>C	ENSP00000405211.1:n.-12G>C
ENST00000455123.5:c.-12G>C	ENSP00000414515.1:n.-12G>C
ENST00000469716.1:n.66G>C
ENST00000469926.5:c.-269G>C	ENSP00000488550.1:n.-269G>C
ENST00000471883.1:n.68G>C
ENST00000490778.5:c.-324G>C	ENSP00000488826.1:n.-324G>C
ENST00000493290.5:c.-345G>C	ENSP00000488822.1:n.-345G>C
ENST00000493469.5:n.1G>C
ENST00000632034.1:c.-12G>C	ENSP00000487898.1:n.-12G>C
ENST00000633192.1:c.52G>C	ENSP00000488378.1:p.Gly18Arg
ENST00000633531.1:c.-12G>C	ENSP00000488838.1:n.-12G>C
NM_000305.2:c.-12G>C	NP_000296.2:n.-12G>C
NM_001018161.1:c.-12G>C	NP_001018171.1:n.-12G>C
XM_005250453.1:c.-190G>C	XP_005250510.1:n.-190G>C
XM_005250454.1:c.-266G>C	XP_005250511.1:n.-266G>C
XM_011516333.1:c.-340G>C	XP_011514635.1:n.-340G>C
XM_017012357.2:c.-266G>C	XP_016867846.1:n.-266G>C
XM_017012358.2:c.-340G>C	XP_016867847.1:n.-340G>C
NM_000305.3:c.-12G>C MANE Select	NP_000296.2:n.-12G>C
NM_001018161.2:c.-12G>C	NP_001018171.1:n.-12G>C