Canonical Allele Identifier: CA162960632

Gene: PON3

Linked Data

• dbSNP Id: rs17878893
• gnomAD v2: 7-95020264-A-G
• gnomAD v3: 7-95390952-A-G
• gnomAD v4: 7-95390952-A-G
• MyVariant Identifiers: chr7:g.95020264A>G (hg19) ; chr7:g.95390952A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95390952A>G , CM000669.2:g.95390952A>G	GRCh38
NC_000007.13:g.95020264A>G , CM000669.1:g.95020264A>G	GRCh37
NC_000007.12:g.94858200A>G	NCBI36
NG_008726.1:g.10424T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265627.10:c.146-743T>C MANE Select	ENSP00000265627.5:n.146-743T>C
ENST00000265627.9:c.146-743T>C	ENSP00000265627.5:n.146-743T>C
ENST00000418617.5:c.*27-743T>C	ENSP00000393174.1:n.*27-743T>C
ENST00000427422.5:c.146-743T>C	ENSP00000413276.1:n.146-743T>C
ENST00000442770.5:c.*27-743T>C	ENSP00000390253.1:n.*27-743T>C
ENST00000451904.5:c.146-743T>C	ENSP00000403850.1:n.146-743T>C
ENST00000456855.5:c.145+3692T>C	ENSP00000391072.1:n.145+3692T>C
ENST00000475439.1:n.334-743T>C
ENST00000482624.5:n.164-743T>C
NM_000940.2:c.146-743T>C	NP_000931.1:n.146-743T>C
NM_000940.3:c.146-743T>C MANE Select	NP_000931.1:n.146-743T>C