Canonical Allele Identifier: CA368237486
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94937361A>T (hg19) chr7:g.95308049A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95308049A>T , CM000669.2:g.95308049A>T GRCh38
NC_000007.13:g.94937361A>T , CM000669.1:g.94937361A>T GRCh37
NC_000007.12:g.94775297A>T NCBI36
NG_008779.1:g.21524T>A
NG_008779.2:g.21658T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.660T>A MANE Select ENSP00000222381.3:p.Phe220Leu
ENST00000222381.7:c.660T>A ENSP00000222381.3:p.Phe220Leu
ENST00000433729.1:c.*385T>A ENSP00000407359.1:n.*385T>A
NM_000446.5:c.660T>A NP_000437.3:p.Phe220Leu
NM_000446.6:c.660T>A NP_000437.3:p.Phe220Leu
NM_000446.7:c.660T>A MANE Select NP_000437.3:p.Phe220Leu
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