Canonical Allele Identifier: CA368244155
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94953729T>C (hg19) chr7:g.95324417T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324417T>C , CM000669.2:g.95324417T>C GRCh38
NC_000007.13:g.94953729T>C , CM000669.1:g.94953729T>C GRCh37
NC_000007.12:g.94791665T>C NCBI36
NG_008779.1:g.5156A>G
NG_008779.2:g.5290A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.59A>G MANE Select ENSP00000222381.3:p.His20Arg
ENST00000222381.7:c.59A>G ENSP00000222381.3:p.His20Arg
ENST00000433729.1:c.59A>G ENSP00000407359.1:p.His20Arg
NM_000446.5:c.59A>G NP_000437.3:p.His20Arg
NM_000446.6:c.59A>G NP_000437.3:p.His20Arg
NM_000446.7:c.59A>G MANE Select NP_000437.3:p.His20Arg
Search 100 bp 5'
Search 100 bp 3'