Canonical Allele Identifier: CA456497435
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94953776C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324464C>G , CM000669.2:g.95324464C>G GRCh38
NC_000007.13:g.94953776C>G , CM000669.1:g.94953776C>G GRCh37
NC_000007.12:g.94791712C>G NCBI36
NG_008779.1:g.5109G>C
NG_008779.2:g.5243G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.12G>C MANE Select ENSP00000222381.3:p.Leu4=
ENST00000222381.7:c.12G>C ENSP00000222381.3:p.Leu4=
ENST00000433729.1:c.12G>C ENSP00000407359.1:p.Leu4=
NM_000446.5:c.12G>C NP_000437.3:p.Leu4=
NM_000446.6:c.12G>C NP_000437.3:p.Leu4=
NM_000446.7:c.12G>C MANE Select NP_000437.3:p.Leu4=
Search 100 bp 5'
Search 100 bp 3'