Canonical Allele Identifier: CA162910688
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs138808374
gnomAD v3: 7-95321277-C-T
gnomAD v4: 7-95321277-C-T
MyVariant Identifiers: chr7:g.94950589C>T (hg19) chr7:g.95321277C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95321277C>T , CM000669.2:g.95321277C>T GRCh38
NC_000007.13:g.94950589C>T , CM000669.1:g.94950589C>T GRCh37
NC_000007.12:g.94788525C>T NCBI36
NG_008779.1:g.8296G>A
NG_008779.2:g.8430G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.75-2884G>A MANE Select ENSP00000222381.3:n.75-2884G>A
ENST00000222381.7:c.75-2884G>A ENSP00000222381.3:n.75-2884G>A
ENST00000433729.1:c.75-2884G>A ENSP00000407359.1:n.75-2884G>A
NM_000446.5:c.75-2884G>A NP_000437.3:n.75-2884G>A
NM_000446.6:c.75-2884G>A NP_000437.3:n.75-2884G>A
NM_000446.7:c.75-2884G>A MANE Select NP_000437.3:n.75-2884G>A
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