Canonical Allele Identifier: CA2683802469
Gene: PON1 HGNC NCBI

Linked Data

gnomAD v4: 7-95307979-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.95307979T>C , CM000669.2:g.95307979T>C GRCh38
NC_000007.13:g.94937291T>C , CM000669.1:g.94937291T>C GRCh37
NC_000007.12:g.94775227T>C NCBI36
NG_008779.1:g.21594A>G
NG_008779.2:g.21728A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222381.8:c.698+32A>G MANE Select ENSP00000222381.3:n.698+32A>G
ENST00000222381.7:c.698+32A>G ENSP00000222381.3:n.698+32A>G
ENST00000433729.1:c.*423+32A>G ENSP00000407359.1:n.*423+32A>G
NM_000446.5:c.698+32A>G NP_000437.3:n.698+32A>G
NM_000446.6:c.698+32A>G NP_000437.3:n.698+32A>G
NM_000446.7:c.698+32A>G MANE Select NP_000437.3:n.698+32A>G