Canonical Allele Identifier: CA045184
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 297692
dbSNP Id: rs564427867
gnomAD v2: 1-55505604-G-A
gnomAD v3: 1-55039931-G-A
gnomAD v4: 1-55039931-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039931G>A , CM000663.2:g.55039931G>A GRCh38
NC_000001.10:g.55505604G>A , CM000663.1:g.55505604G>A GRCh37
NC_000001.9:g.55278192G>A NCBI36
NG_009061.1:g.5385G>A , LRG_275:g.5385G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.94G>A ENSP00000501161.2:p.Glu32Lys
ENST00000710286.1:c.451G>A ENSP00000518176.1:p.Glu151Lys
ENST00000673726.1:c.94G>A ENSP00000501004.1:p.Glu32Lys
ENST00000302118.5:c.94G>A MANE Select ENSP00000303208.5:p.Glu32Lys
NM_174936.3:c.94G>A , LRG_275t1:c.94G>A NP_777596.2:p.Glu32Lys
NM_174936.4:c.94G>A MANE Select NP_777596.2:p.Glu32Lys