Canonical Allele Identifier: CA1727231351
Gene: PON3 HGNC NCBI

Linked Data

dbSNP Id: rs1809305387
gnomAD v3: 7-95390961-C-A
gnomAD v4: 7-95390961-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95390961C>A , CM000669.2:g.95390961C>A GRCh38
NC_000007.13:g.95020273C>A , CM000669.1:g.95020273C>A GRCh37
NC_000007.12:g.94858209C>A NCBI36
NG_008726.1:g.10415G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265627.10:c.146-752G>T MANE Select ENSP00000265627.5:n.146-752G>T
ENST00000265627.9:c.146-752G>T ENSP00000265627.5:n.146-752G>T
ENST00000418617.5:c.*27-752G>T ENSP00000393174.1:n.*27-752G>T
ENST00000427422.5:c.146-752G>T ENSP00000413276.1:n.146-752G>T
ENST00000442770.5:c.*27-752G>T ENSP00000390253.1:n.*27-752G>T
ENST00000451904.5:c.146-752G>T ENSP00000403850.1:n.146-752G>T
ENST00000456855.5:c.145+3683G>T ENSP00000391072.1:n.145+3683G>T
ENST00000475439.1:n.334-752G>T
ENST00000482624.5:n.164-752G>T
NM_000940.2:c.146-752G>T NP_000931.1:n.146-752G>T
NM_000940.3:c.146-752G>T MANE Select NP_000931.1:n.146-752G>T