Canonical Allele Identifier: CA844124902

Gene: PON3

Linked Data

• dbSNP Id: rs1263999503
• gnomAD v3: 7-95390941-C-A
• gnomAD v4: 7-95390941-C-A
• MyVariant Identifiers: chr7:g.95020253C>A (hg19) ; chr7:g.95390941C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.95390941C>A , CM000669.2:g.95390941C>A	GRCh38
NC_000007.13:g.95020253C>A , CM000669.1:g.95020253C>A	GRCh37
NC_000007.12:g.94858189C>A	NCBI36
NG_008726.1:g.10435G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265627.10:c.146-732G>T MANE Select	ENSP00000265627.5:n.146-732G>T
ENST00000265627.9:c.146-732G>T	ENSP00000265627.5:n.146-732G>T
ENST00000418617.5:c.*27-732G>T	ENSP00000393174.1:n.*27-732G>T
ENST00000427422.5:c.146-732G>T	ENSP00000413276.1:n.146-732G>T
ENST00000442770.5:c.*27-732G>T	ENSP00000390253.1:n.*27-732G>T
ENST00000451904.5:c.146-732G>T	ENSP00000403850.1:n.146-732G>T
ENST00000456855.5:c.145+3703G>T	ENSP00000391072.1:n.145+3703G>T
ENST00000475439.1:n.334-732G>T
ENST00000482624.5:n.164-732G>T
NM_000940.2:c.146-732G>T	NP_000931.1:n.146-732G>T
NM_000940.3:c.146-732G>T MANE Select	NP_000931.1:n.146-732G>T