Canonical Allele Identifier: CA340482739
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 874403
dbSNP Id: rs866597555

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039922C>G , CM000663.2:g.55039922C>G GRCh38
NC_000001.10:g.55505595C>G , CM000663.1:g.55505595C>G GRCh37
NC_000001.9:g.55278183C>G NCBI36
NG_009061.1:g.5376C>G , LRG_275:g.5376C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.85C>G ENSP00000501161.2:p.Arg29Gly
ENST00000710286.1:c.442C>G ENSP00000518176.1:p.Arg148Gly
ENST00000673726.1:c.85C>G ENSP00000501004.1:p.Arg29Gly
ENST00000302118.5:c.85C>G MANE Select ENSP00000303208.5:p.Arg29Gly
NM_174936.3:c.85C>G , LRG_275t1:c.85C>G NP_777596.2:p.Arg29Gly
NM_174936.4:c.85C>G MANE Select NP_777596.2:p.Arg29Gly