Canonical Allele Identifier: CA340482623
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 628031
ClinVar RCV Id: RCV000772311 RCV003605680
dbSNP Id: rs1426361407
gnomAD v2: 1-55505532-C-T
gnomAD v3: 1-55039859-C-T
gnomAD v4: 1-55039859-C-T
MyVariant Identifiers: chr1:g.55505532C>T (hg19) chr1:g.55039859C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039859C>T , CM000663.2:g.55039859C>T GRCh38
NC_000001.10:g.55505532C>T , CM000663.1:g.55505532C>T GRCh37
NC_000001.9:g.55278120C>T NCBI36
NG_009061.1:g.5313C>T , LRG_275:g.5313C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.22C>T ENSP00000501161.2:p.Arg8Trp
ENST00000710286.1:c.379C>T ENSP00000518176.1:p.Arg127Trp
ENST00000673726.1:c.22C>T ENSP00000501004.1:p.Arg8Trp
ENST00000302118.5:c.22C>T MANE Select ENSP00000303208.5:p.Arg8Trp
NM_174936.3:c.22C>T , LRG_275t1:c.22C>T NP_777596.2:p.Arg8Trp
NM_174936.4:c.22C>T MANE Select NP_777596.2:p.Arg8Trp
Search 100 bp 5'
Search 100 bp 3'