Canonical Allele Identifier: CA456495287
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94937364T>G (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000222381.8:c.657A>C MANE Select ENSP00000222381.3:p.Gly219=
ENST00000222381.7:c.657A>C ENSP00000222381.3:p.Gly219=
ENST00000433729.1:c.*382A>C ENSP00000407359.1:n.*382A>C
NM_000446.5:c.657A>C NP_000437.3:p.Gly219=
NM_000446.6:c.657A>C NP_000437.3:p.Gly219=
NM_000446.7:c.657A>C MANE Select NP_000437.3:p.Gly219=
Search 100 bp 5'
Search 100 bp 3'