Canonical Allele Identifier: CA1727231311
Gene: PON3 HGNC NCBI

Linked Data

dbSNP Id: rs1809304587

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95390906A>G , CM000669.2:g.95390906A>G GRCh38
NC_000007.13:g.95020218A>G , CM000669.1:g.95020218A>G GRCh37
NC_000007.12:g.94858154A>G NCBI36
NG_008726.1:g.10470T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265627.10:c.146-697T>C MANE Select ENSP00000265627.5:n.146-697T>C
ENST00000265627.9:c.146-697T>C ENSP00000265627.5:n.146-697T>C
ENST00000418617.5:c.*27-697T>C ENSP00000393174.1:n.*27-697T>C
ENST00000427422.5:c.146-697T>C ENSP00000413276.1:n.146-697T>C
ENST00000442770.5:c.*27-697T>C ENSP00000390253.1:n.*27-697T>C
ENST00000451904.5:c.146-697T>C ENSP00000403850.1:n.146-697T>C
ENST00000456855.5:c.145+3738T>C ENSP00000391072.1:n.145+3738T>C
ENST00000475439.1:n.334-697T>C
ENST00000482624.5:n.164-697T>C
NM_000940.2:c.146-697T>C NP_000931.1:n.146-697T>C
NM_000940.3:c.146-697T>C MANE Select NP_000931.1:n.146-697T>C