Canonical Allele Identifier: CA340482722
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 440705
ClinVar RCV Id: RCV000508903 RCV004023448
dbSNP Id: rs1553135400
gnomAD v3: 1-55039913-G-A
gnomAD v4: 1-55039913-G-A
MyVariant Identifiers: chr1:g.55505586G>A (hg19) chr1:g.55039913G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039913G>A , CM000663.2:g.55039913G>A GRCh38
NC_000001.10:g.55505586G>A , CM000663.1:g.55505586G>A GRCh37
NC_000001.9:g.55278174G>A NCBI36
NG_009061.1:g.5367G>A , LRG_275:g.5367G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.76G>A ENSP00000501161.2:p.Ala26Thr
ENST00000710286.1:c.433G>A ENSP00000518176.1:p.Ala145Thr
ENST00000673726.1:c.76G>A ENSP00000501004.1:p.Ala26Thr
ENST00000302118.5:c.76G>A MANE Select ENSP00000303208.5:p.Ala26Thr
NM_174936.3:c.76G>A , LRG_275t1:c.76G>A NP_777596.2:p.Ala26Thr
NM_174936.4:c.76G>A MANE Select NP_777596.2:p.Ala26Thr
Search 100 bp 5'
Search 100 bp 3'