Canonical Allele Identifier: CA162961679
Gene: PON3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95392491T>C , CM000669.2:g.95392491T>C GRCh38
NC_000007.13:g.95021803T>C , CM000669.1:g.95021803T>C GRCh37
NC_000007.12:g.94859739T>C NCBI36
NG_008726.1:g.8885A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265627.10:c.145+2153A>G MANE Select ENSP00000265627.5:n.145+2153A>G
ENST00000265627.9:c.145+2153A>G ENSP00000265627.5:n.145+2153A>G
ENST00000418617.5:c.*26+2153A>G ENSP00000393174.1:n.*26+2153A>G
ENST00000427422.5:c.145+2153A>G ENSP00000413276.1:n.145+2153A>G
ENST00000442770.5:c.*26+2153A>G ENSP00000390253.1:n.*26+2153A>G
ENST00000451904.5:c.145+2153A>G ENSP00000403850.1:n.145+2153A>G
ENST00000456855.5:c.145+2153A>G ENSP00000391072.1:n.145+2153A>G
ENST00000475439.1:n.333+2153A>G
ENST00000482624.5:n.163+2153A>G
NM_000940.2:c.145+2153A>G NP_000931.1:n.145+2153A>G
NM_000940.3:c.145+2153A>G MANE Select NP_000931.1:n.145+2153A>G