Canonical Allele Identifier: CA576332690

Gene: PON2

Linked Data

• dbSNP Id: rs936595873
• gnomAD v2: 7-95064186-C-G
• gnomAD v4: 7-95434874-C-G
• MyVariant Identifiers: chr7:g.95064186C>G (hg19) ; chr7:g.95434874C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95434874C>G , CM000669.2:g.95434874C>G	GRCh38
NC_000007.13:g.95064186C>G , CM000669.1:g.95064186C>G	GRCh37
NC_000007.12:g.94902122C>G	NCBI36
NG_008725.1:g.5199G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222572.8:c.74+4G>C MANE Select	ENSP00000222572.3:n.74+4G>C
ENST00000222572.7:c.74+4G>C	ENSP00000222572.3:n.74+4G>C
ENST00000433091.6:c.74+4G>C	ENSP00000404622.2:n.74+4G>C
ENST00000446142.5:c.74+4G>C	ENSP00000405211.1:n.74+4G>C
ENST00000455123.5:c.74+4G>C	ENSP00000414515.1:n.74+4G>C
ENST00000460873.5:n.74+4G>C
ENST00000469716.1:n.151+4G>C
ENST00000469926.5:c.-184+4G>C	ENSP00000488550.1:n.-184+4G>C
ENST00000471883.1:n.153+4G>C
ENST00000478801.5:c.-385+4G>C	ENSP00000487703.1:n.-385+4G>C
ENST00000490778.5:c.-239+4G>C	ENSP00000488826.1:n.-239+4G>C
ENST00000491069.5:c.74+4G>C	ENSP00000488462.1:n.74+4G>C
ENST00000493290.5:c.-260+4G>C	ENSP00000488822.1:n.-260+4G>C
ENST00000493469.5:n.86+4G>C
ENST00000632034.1:c.74+4G>C	ENSP00000487898.1:n.74+4G>C
ENST00000633192.1:c.137+4G>C	ENSP00000488378.1:n.137+4G>C
ENST00000633531.1:c.74+4G>C	ENSP00000488838.1:n.74+4G>C
NM_000305.2:c.74+4G>C	NP_000296.2:n.74+4G>C
NM_001018161.1:c.74+4G>C	NP_001018171.1:n.74+4G>C
XM_005250453.1:c.-105+4G>C	XP_005250510.1:n.-105+4G>C
XM_005250454.1:c.-181+4G>C	XP_005250511.1:n.-181+4G>C
XM_011516333.1:c.-255+4G>C	XP_011514635.1:n.-255+4G>C
XM_017012357.2:c.-181+4G>C	XP_016867846.1:n.-181+4G>C
XM_017012358.2:c.-255+4G>C	XP_016867847.1:n.-255+4G>C
NM_000305.3:c.74+4G>C MANE Select	NP_000296.2:n.74+4G>C
NM_001018161.2:c.74+4G>C	NP_001018171.1:n.74+4G>C