Canonical Allele Identifier: CA456497401
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs2116333732
MyVariant Identifiers: chr7:g.94953725C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324413C>T , CM000669.2:g.95324413C>T GRCh38
NC_000007.13:g.94953725C>T , CM000669.1:g.94953725C>T GRCh37
NC_000007.12:g.94791661C>T NCBI36
NG_008779.1:g.5160G>A
NG_008779.2:g.5294G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.63G>A MANE Select ENSP00000222381.3:p.Gln21=
ENST00000222381.7:c.63G>A ENSP00000222381.3:p.Gln21=
ENST00000433729.1:c.63G>A ENSP00000407359.1:p.Gln21=
NM_000446.5:c.63G>A NP_000437.3:p.Gln21=
NM_000446.6:c.63G>A NP_000437.3:p.Gln21=
NM_000446.7:c.63G>A MANE Select NP_000437.3:p.Gln21=
Search 100 bp 5'
Search 100 bp 3'