Canonical Allele Identifier: CA162954001

Gene: PON2

Linked Data

• dbSNP Id: rs1046553958
• gnomAD v2: 7-95064271-G-A
• gnomAD v3: 7-95434959-G-A
• gnomAD v4: 7-95434959-G-A
• MyVariant Identifiers: chr7:g.95064271G>A (hg19) ; chr7:g.95434959G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434959G>A , CM000669.2:g.95434959G>A	GRCh38
NC_000007.13:g.95064271G>A , CM000669.1:g.95064271G>A	GRCh37
NC_000007.12:g.94902207G>A	NCBI36
NG_008725.1:g.5114C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222572.8:c.-8C>T MANE Select	ENSP00000222572.3:n.-8C>T
ENST00000222572.7:c.-8C>T	ENSP00000222572.3:n.-8C>T
ENST00000433091.6:c.-8C>T	ENSP00000404622.2:n.-8C>T
ENST00000446142.5:c.-8C>T	ENSP00000405211.1:n.-8C>T
ENST00000455123.5:c.-8C>T	ENSP00000414515.1:n.-8C>T
ENST00000469716.1:n.70C>T
ENST00000469926.5:c.-265C>T	ENSP00000488550.1:n.-265C>T
ENST00000471883.1:n.72C>T
ENST00000490778.5:c.-320C>T	ENSP00000488826.1:n.-320C>T
ENST00000493290.5:c.-341C>T	ENSP00000488822.1:n.-341C>T
ENST00000493469.5:n.5C>T
ENST00000632034.1:c.-8C>T	ENSP00000487898.1:n.-8C>T
ENST00000633192.1:c.56C>T	ENSP00000488378.1:p.Ser19Phe
ENST00000633531.1:c.-8C>T	ENSP00000488838.1:n.-8C>T
NM_000305.2:c.-8C>T	NP_000296.2:n.-8C>T
NM_001018161.1:c.-8C>T	NP_001018171.1:n.-8C>T
XM_005250453.1:c.-186C>T	XP_005250510.1:n.-186C>T
XM_005250454.1:c.-262C>T	XP_005250511.1:n.-262C>T
XM_011516333.1:c.-336C>T	XP_011514635.1:n.-336C>T
XM_017012357.2:c.-262C>T	XP_016867846.1:n.-262C>T
XM_017012358.2:c.-336C>T	XP_016867847.1:n.-336C>T
NM_000305.3:c.-8C>T MANE Select	NP_000296.2:n.-8C>T
NM_001018161.2:c.-8C>T	NP_001018171.1:n.-8C>T