Canonical Allele Identifier: CA162897811
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs955951277
MyVariant Identifiers: chr7:g.94934602T>A (hg19) chr7:g.95305290T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95305290T>A , CM000669.2:g.95305290T>A GRCh38
NC_000007.13:g.94934602T>A , CM000669.1:g.94934602T>A GRCh37
NC_000007.12:g.94772538T>A NCBI36
NG_008779.1:g.24283A>T
NG_008779.2:g.24417A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000222381.8:c.780+995A>T MANE Select ENSP00000222381.3:n.780+995A>T
ENST00000222381.7:c.780+995A>T ENSP00000222381.3:n.780+995A>T
ENST00000433729.1:c.*505+995A>T ENSP00000407359.1:n.*505+995A>T
NM_000446.5:c.780+995A>T NP_000437.3:n.780+995A>T
NM_000446.6:c.780+995A>T NP_000437.3:n.780+995A>T
NM_000446.7:c.780+995A>T MANE Select NP_000437.3:n.780+995A>T
Search 100 bp 5'
Search 100 bp 3'