Canonical Allele Identifier: CA456497406
Gene: PON1 HGNC NCBI

Linked Data

gnomAD v4: 7-95324428-G-C
MyVariant Identifiers: chr7:g.94953740G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324428G>C , CM000669.2:g.95324428G>C GRCh38
NC_000007.13:g.94953740G>C , CM000669.1:g.94953740G>C GRCh37
NC_000007.12:g.94791676G>C NCBI36
NG_008779.1:g.5145C>G
NG_008779.2:g.5279C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.48C>G MANE Select ENSP00000222381.3:p.Leu16=
ENST00000222381.7:c.48C>G ENSP00000222381.3:p.Leu16=
ENST00000433729.1:c.48C>G ENSP00000407359.1:p.Leu16=
NM_000446.5:c.48C>G NP_000437.3:p.Leu16=
NM_000446.6:c.48C>G NP_000437.3:p.Leu16=
NM_000446.7:c.48C>G MANE Select NP_000437.3:p.Leu16=