Canonical Allele Identifier: CA368244196
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94953750C>A (hg19) chr7:g.95324438C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324438C>A , CM000669.2:g.95324438C>A GRCh38
NC_000007.13:g.94953750C>A , CM000669.1:g.94953750C>A GRCh37
NC_000007.12:g.94791686C>A NCBI36
NG_008779.1:g.5135G>T
NG_008779.2:g.5269G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.38G>T MANE Select ENSP00000222381.3:p.Gly13Val
ENST00000222381.7:c.38G>T ENSP00000222381.3:p.Gly13Val
ENST00000433729.1:c.38G>T ENSP00000407359.1:p.Gly13Val
NM_000446.5:c.38G>T NP_000437.3:p.Gly13Val
NM_000446.6:c.38G>T NP_000437.3:p.Gly13Val
NM_000446.7:c.38G>T MANE Select NP_000437.3:p.Gly13Val
Search 100 bp 5'
Search 100 bp 3'