Canonical Allele Identifier: CA1104657725
Gene: PON1 HGNC NCBI

Linked Data

dbSNP Id: rs1807892149
gnomAD v3: 7-95321320-T-C
gnomAD v4: 7-95321320-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95321320T>C , CM000669.2:g.95321320T>C GRCh38
NC_000007.13:g.94950632T>C , CM000669.1:g.94950632T>C GRCh37
NC_000007.12:g.94788568T>C NCBI36
NG_008779.1:g.8253A>G
NG_008779.2:g.8387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.75-2927A>G MANE Select ENSP00000222381.3:n.75-2927A>G
ENST00000222381.7:c.75-2927A>G ENSP00000222381.3:n.75-2927A>G
ENST00000433729.1:c.75-2927A>G ENSP00000407359.1:n.75-2927A>G
NM_000446.5:c.75-2927A>G NP_000437.3:n.75-2927A>G
NM_000446.6:c.75-2927A>G NP_000437.3:n.75-2927A>G
NM_000446.7:c.75-2927A>G MANE Select NP_000437.3:n.75-2927A>G
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