Canonical Allele Identifier: CA417957332
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55039918-C-A
MyVariant Identifiers: chr1:g.55505591C>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.81C>A ENSP00000501161.2:p.Gly27=
ENST00000710286.1:c.438C>A ENSP00000518176.1:p.Gly146=
ENST00000673726.1:c.81C>A ENSP00000501004.1:p.Gly27=
ENST00000302118.5:c.81C>A MANE Select ENSP00000303208.5:p.Gly27=
NM_174936.3:c.81C>A , LRG_275t1:c.81C>A NP_777596.2:p.Gly27=
NM_174936.4:c.81C>A MANE Select NP_777596.2:p.Gly27=
Search 100 bp 5'
Search 100 bp 3'