Canonical Allele Identifier: CA456497396
Gene: PON1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94953719A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324407A>G , CM000669.2:g.95324407A>G GRCh38
NC_000007.13:g.94953719A>G , CM000669.1:g.94953719A>G GRCh37
NC_000007.12:g.94791655A>G NCBI36
NG_008779.1:g.5166T>C
NG_008779.2:g.5300T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.69T>C MANE Select ENSP00000222381.3:p.Ser23=
ENST00000222381.7:c.69T>C ENSP00000222381.3:p.Ser23=
ENST00000433729.1:c.69T>C ENSP00000407359.1:p.Ser23=
NM_000446.5:c.69T>C NP_000437.3:p.Ser23=
NM_000446.6:c.69T>C NP_000437.3:p.Ser23=
NM_000446.7:c.69T>C MANE Select NP_000437.3:p.Ser23=