Canonical Allele Identifier: CA170540
Gene: PON1 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.95324583G>A
GRCh37 chr7:g.94953895G>A
gnomAD v2:
7:94953895 G / A
gnomAD v3:
7:95324583 G / A
gnomAD v4:
chr7-95324583-G-A
Joint Max Group AF 0.47536417 (MID)
Genomes Max Group AF 0.47581429 (NFE)
Exomes Max Group AF 0.47461246 (NFE)
ClinVar RCV:
RCV000133466
RCV001650832
ClinVar Variation:
13737
dbSNP:
705379
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324583G>A , CM000669.2:g.95324583G>A GRCh38
NC_000007.13:g.94953895G>A , CM000669.1:g.94953895G>A GRCh37
NC_000007.12:g.94791831G>A NCBI36
NG_008779.1:g.4990C>T
NG_008779.2:g.5124C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.7:c.-108C>T ENSP00000222381.3:n.-108C>T
NM_000446.6:c.-108C>T NP_000437.3:n.-108C>T
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