Canonical Allele Identifier: CA368237488
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94937362A>C (hg19) chr7:g.95308050A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95308050A>C , CM000669.2:g.95308050A>C GRCh38
NC_000007.13:g.94937362A>C , CM000669.1:g.94937362A>C GRCh37
NC_000007.12:g.94775298A>C NCBI36
NG_008779.1:g.21523T>G
NG_008779.2:g.21657T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.659T>G MANE Select ENSP00000222381.3:p.Phe220Cys
ENST00000222381.7:c.659T>G ENSP00000222381.3:p.Phe220Cys
ENST00000433729.1:c.*384T>G ENSP00000407359.1:n.*384T>G
NM_000446.5:c.659T>G NP_000437.3:p.Phe220Cys
NM_000446.6:c.659T>G NP_000437.3:p.Phe220Cys
NM_000446.7:c.659T>G MANE Select NP_000437.3:p.Phe220Cys
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