Canonical Allele Identifier: CA162912825
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs944217516
gnomAD v3: 7-95324287-A-G
gnomAD v4: 7-95324287-A-G
MyVariant Identifiers: chr7:g.94953599A>G (hg19) chr7:g.95324287A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324287A>G , CM000669.2:g.95324287A>G GRCh38
NC_000007.13:g.94953599A>G , CM000669.1:g.94953599A>G GRCh37
NC_000007.12:g.94791535A>G NCBI36
NG_008779.1:g.5286T>C
NG_008779.2:g.5420T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.74+115T>C MANE Select ENSP00000222381.3:n.74+115T>C
ENST00000222381.7:c.74+115T>C ENSP00000222381.3:n.74+115T>C
ENST00000433729.1:c.74+115T>C ENSP00000407359.1:n.74+115T>C
NM_000446.5:c.74+115T>C NP_000437.3:n.74+115T>C
NM_000446.6:c.74+115T>C NP_000437.3:n.74+115T>C
NM_000446.7:c.74+115T>C MANE Select NP_000437.3:n.74+115T>C
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