Canonical Allele Identifier: CA456497402
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94953728G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324416G>A , CM000669.2:g.95324416G>A GRCh38
NC_000007.13:g.94953728G>A , CM000669.1:g.94953728G>A GRCh37
NC_000007.12:g.94791664G>A NCBI36
NG_008779.1:g.5157C>T
NG_008779.2:g.5291C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.60C>T MANE Select ENSP00000222381.3:p.His20=
ENST00000222381.7:c.60C>T ENSP00000222381.3:p.His20=
ENST00000433729.1:c.60C>T ENSP00000407359.1:p.His20=
NM_000446.5:c.60C>T NP_000437.3:p.His20=
NM_000446.6:c.60C>T NP_000437.3:p.His20=
NM_000446.7:c.60C>T MANE Select NP_000437.3:p.His20=