Canonical Allele Identifier: CA456495291
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs1807576475
gnomAD v4: 7-95308058-T-C
MyVariant Identifiers: chr7:g.94937370T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95308058T>C , CM000669.2:g.95308058T>C GRCh38
NC_000007.13:g.94937370T>C , CM000669.1:g.94937370T>C GRCh37
NC_000007.12:g.94775306T>C NCBI36
NG_008779.1:g.21515A>G
NG_008779.2:g.21649A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.651A>G MANE Select ENSP00000222381.3:p.Ala217=
ENST00000222381.7:c.651A>G ENSP00000222381.3:p.Ala217=
ENST00000433729.1:c.*376A>G ENSP00000407359.1:n.*376A>G
NM_000446.5:c.651A>G NP_000437.3:p.Ala217=
NM_000446.6:c.651A>G NP_000437.3:p.Ala217=
NM_000446.7:c.651A>G MANE Select NP_000437.3:p.Ala217=