Canonical Allele Identifier: CA162912901
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs963697365
gnomAD v2: 7-94953681-G-A
gnomAD v3: 7-95324369-G-A
gnomAD v4: 7-95324369-G-A
MyVariant Identifiers: chr7:g.94953681G>A (hg19) chr7:g.95324369G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324369G>A , CM000669.2:g.95324369G>A GRCh38
NC_000007.13:g.94953681G>A , CM000669.1:g.94953681G>A GRCh37
NC_000007.12:g.94791617G>A NCBI36
NG_008779.1:g.5204C>T
NG_008779.2:g.5338C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.74+33C>T MANE Select ENSP00000222381.3:n.74+33C>T
ENST00000222381.7:c.74+33C>T ENSP00000222381.3:n.74+33C>T
ENST00000433729.1:c.74+33C>T ENSP00000407359.1:n.74+33C>T
NM_000446.5:c.74+33C>T NP_000437.3:n.74+33C>T
NM_000446.6:c.74+33C>T NP_000437.3:n.74+33C>T
NM_000446.7:c.74+33C>T MANE Select NP_000437.3:n.74+33C>T
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