Canonical Allele Identifier: CA456495286
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94937364T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95308052T>A , CM000669.2:g.95308052T>A GRCh38
NC_000007.13:g.94937364T>A , CM000669.1:g.94937364T>A GRCh37
NC_000007.12:g.94775300T>A NCBI36
NG_008779.1:g.21521A>T
NG_008779.2:g.21655A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.657A>T MANE Select ENSP00000222381.3:p.Gly219=
ENST00000222381.7:c.657A>T ENSP00000222381.3:p.Gly219=
ENST00000433729.1:c.*382A>T ENSP00000407359.1:n.*382A>T
NM_000446.5:c.657A>T NP_000437.3:p.Gly219=
NM_000446.6:c.657A>T NP_000437.3:p.Gly219=
NM_000446.7:c.657A>T MANE Select NP_000437.3:p.Gly219=