Canonical Allele Identifier: CA576340649

Gene: PON3

Linked Data

• dbSNP Id: rs1424509723
• gnomAD v2: 7-95020276-A-G
• gnomAD v3: 7-95390964-A-G
• gnomAD v4: 7-95390964-A-G
• MyVariant Identifiers: chr7:g.95020276A>G (hg19) ; chr7:g.95390964A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95390964A>G , CM000669.2:g.95390964A>G	GRCh38
NC_000007.13:g.95020276A>G , CM000669.1:g.95020276A>G	GRCh37
NC_000007.12:g.94858212A>G	NCBI36
NG_008726.1:g.10412T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265627.10:c.146-755T>C MANE Select	ENSP00000265627.5:n.146-755T>C
ENST00000265627.9:c.146-755T>C	ENSP00000265627.5:n.146-755T>C
ENST00000418617.5:c.*27-755T>C	ENSP00000393174.1:n.*27-755T>C
ENST00000427422.5:c.146-755T>C	ENSP00000413276.1:n.146-755T>C
ENST00000442770.5:c.*27-755T>C	ENSP00000390253.1:n.*27-755T>C
ENST00000451904.5:c.146-755T>C	ENSP00000403850.1:n.146-755T>C
ENST00000456855.5:c.145+3680T>C	ENSP00000391072.1:n.145+3680T>C
ENST00000475439.1:n.334-755T>C
ENST00000482624.5:n.164-755T>C
NM_000940.2:c.146-755T>C	NP_000931.1:n.146-755T>C
NM_000940.3:c.146-755T>C MANE Select	NP_000931.1:n.146-755T>C