Canonical Allele Identifier: CA10654837
Gene: PCSK9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 369876
ClinVar RCV Id: RCV000408784
dbSNP Id: rs1057516136

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059519A>G , CM000663.2:g.55059519A>G GRCh38
NC_000001.10:g.55525192A>G , CM000663.1:g.55525192A>G GRCh37
NC_000001.9:g.55297780A>G NCBI36
NG_009061.1:g.24973A>G , LRG_275:g.24973A>G

Transcript Alleles

HGVS Amino-acid change
NM_174936.3:c.1537A>G , LRG_275t1:c.1537A>G NP_777596.2:p.Asn513Asp
NR_110451.1:n.1144A>G
XM_011541193.1:c.658A>G XP_011539495.1:p.Asn220Asp
ENST00000302118.5:c.1537A>G ENSP00000303208.5:p.Asn513Asp
ENST00000490692.1:n.2227+872A>G