Canonical Allele Identifier: CA162908646
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs551167661
gnomAD v2: 7-94947784-A-C
gnomAD v3: 7-95318472-A-C
gnomAD v4: 7-95318472-A-C
MyVariant Identifiers: chr7:g.94947784A>C (hg19) chr7:g.95318472A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95318472A>C , CM000669.2:g.95318472A>C GRCh38
NC_000007.13:g.94947784A>C , CM000669.1:g.94947784A>C GRCh37
NC_000007.12:g.94785720A>C NCBI36
NG_008779.1:g.11101T>G
NG_008779.2:g.11235T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.75-79T>G MANE Select ENSP00000222381.3:n.75-79T>G
ENST00000222381.7:c.75-79T>G ENSP00000222381.3:n.75-79T>G
ENST00000433729.1:c.75-79T>G ENSP00000407359.1:n.75-79T>G
ENST00000470502.1:n.116T>G
NM_000446.5:c.75-79T>G NP_000437.3:n.75-79T>G
NM_000446.6:c.75-79T>G NP_000437.3:n.75-79T>G
NM_000446.7:c.75-79T>G MANE Select NP_000437.3:n.75-79T>G
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