Canonical Allele Identifier: CA737022755
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1351851735

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039627A>G , CM000663.2:g.55039627A>G GRCh38
NC_000001.10:g.55505300A>G , CM000663.1:g.55505300A>G GRCh37
NC_000001.9:g.55277888A>G NCBI36
NG_009061.1:g.5081A>G , LRG_275:g.5081A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.-211A>G ENSP00000501161.2:n.-211A>G
ENST00000710286.1:c.147A>G ENSP00000518176.1:p.Ala49=
ENST00000673726.1:c.-211A>G ENSP00000501004.1:n.-211A>G
ENST00000302118.5:c.-211A>G MANE Select ENSP00000303208.5:n.-211A>G
NM_174936.3:c.-211A>G , LRG_275t1:c.-211A>G NP_777596.2:n.-211A>G
NM_174936.4:c.-211A>G MANE Select NP_777596.2:n.-211A>G