Canonical Allele Identifier: CA340483778
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1351049773

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043980C>A , CM000663.2:g.55043980C>A GRCh38
NC_000001.10:g.55509653C>A , CM000663.1:g.55509653C>A GRCh37
NC_000001.9:g.55282241C>A NCBI36
NG_009061.1:g.9434C>A , LRG_275:g.9434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.345C>A ENSP00000501161.2:p.Phe115Leu
ENST00000710286.1:c.702C>A ENSP00000518176.1:p.Phe234Leu
ENST00000673662.1:n.15C>A
ENST00000673726.1:c.345C>A ENSP00000501004.1:p.Phe115Leu
ENST00000673903.1:c.-31C>A ENSP00000501257.1:n.-31C>A
ENST00000302118.5:c.345C>A MANE Select ENSP00000303208.5:p.Phe115Leu
NM_174936.3:c.345C>A , LRG_275t1:c.345C>A NP_777596.2:p.Phe115Leu
NR_110451.1:n.182+3577C>A
NM_174936.4:c.345C>A MANE Select NP_777596.2:p.Phe115Leu
NR_110451.2:n.182+3577C>A