Canonical Allele Identifier: CA368244204
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs1807968954
MyVariant Identifiers: chr7:g.94953753A>G (hg19) chr7:g.95324441A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95324441A>G , CM000669.2:g.95324441A>G GRCh38
NC_000007.13:g.94953753A>G , CM000669.1:g.94953753A>G GRCh37
NC_000007.12:g.94791689A>G NCBI36
NG_008779.1:g.5132T>C
NG_008779.2:g.5266T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.35T>C MANE Select ENSP00000222381.3:p.Met12Thr
ENST00000222381.7:c.35T>C ENSP00000222381.3:p.Met12Thr
ENST00000433729.1:c.35T>C ENSP00000407359.1:p.Met12Thr
NM_000446.5:c.35T>C NP_000437.3:p.Met12Thr
NM_000446.6:c.35T>C NP_000437.3:p.Met12Thr
NM_000446.7:c.35T>C MANE Select NP_000437.3:p.Met12Thr
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