Canonical Allele Identifier: CA340483588
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 629199
dbSNP Id: rs1557499351

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043882A>G , CM000663.2:g.55043882A>G GRCh38
NC_000001.10:g.55509555A>G , CM000663.1:g.55509555A>G GRCh37
NC_000001.9:g.55282143A>G NCBI36
NG_009061.1:g.9336A>G , LRG_275:g.9336A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.247A>G ENSP00000501161.2:p.Lys83Glu
ENST00000710286.1:c.604A>G ENSP00000518176.1:p.Lys202Glu
ENST00000673726.1:c.247A>G ENSP00000501004.1:p.Lys83Glu
ENST00000673903.1:c.-129A>G ENSP00000501257.1:n.-129A>G
ENST00000302118.5:c.247A>G MANE Select ENSP00000303208.5:p.Lys83Glu
NM_174936.3:c.247A>G , LRG_275t1:c.247A>G NP_777596.2:p.Lys83Glu
NR_110451.1:n.182+3479A>G
NM_174936.4:c.247A>G MANE Select NP_777596.2:p.Lys83Glu
NR_110451.2:n.182+3479A>G