Canonical Allele Identifier: CA417957333
Gene: PCSK9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55505591C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039918C>G , CM000663.2:g.55039918C>G GRCh38
NC_000001.10:g.55505591C>G , CM000663.1:g.55505591C>G GRCh37
NC_000001.9:g.55278179C>G NCBI36
NG_009061.1:g.5372C>G , LRG_275:g.5372C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.81C>G ENSP00000501161.2:p.Gly27=
ENST00000710286.1:c.438C>G ENSP00000518176.1:p.Gly146=
ENST00000673726.1:c.81C>G ENSP00000501004.1:p.Gly27=
ENST00000302118.5:c.81C>G MANE Select ENSP00000303208.5:p.Gly27=
NM_174936.3:c.81C>G , LRG_275t1:c.81C>G NP_777596.2:p.Gly27=
NM_174936.4:c.81C>G MANE Select NP_777596.2:p.Gly27=