Canonical Allele Identifier: CA1167978183
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644617232

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55044064C>G , CM000663.2:g.55044064C>G GRCh38
NC_000001.10:g.55509737C>G , CM000663.1:g.55509737C>G GRCh37
NC_000001.9:g.55282325C>G NCBI36
NG_009061.1:g.9518C>G , LRG_275:g.9518C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.399+30C>G ENSP00000501161.2:n.399+30C>G
ENST00000710286.1:c.756+30C>G ENSP00000518176.1:n.756+30C>G
ENST00000673662.1:n.69+30C>G
ENST00000673726.1:c.399+30C>G ENSP00000501004.1:n.399+30C>G
ENST00000673903.1:c.24+30C>G ENSP00000501257.1:n.24+30C>G
ENST00000302118.5:c.399+30C>G MANE Select ENSP00000303208.5:n.399+30C>G
NM_174936.3:c.399+30C>G , LRG_275t1:c.399+30C>G NP_777596.2:n.399+30C>G
NR_110451.1:n.182+3661C>G
NM_174936.4:c.399+30C>G MANE Select NP_777596.2:n.399+30C>G
NR_110451.2:n.182+3661C>G