Canonical Allele Identifier: CA10611300
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 297716
ClinVar RCV Id: RCV000294144 RCV001101552 RCV002274977
dbSNP Id: rs557622245
gnomAD v2: 1-55529428-C-T
gnomAD v3: 1-55063755-C-T
gnomAD v4: 1-55063755-C-T
MyVariant Identifiers: chr1:g.55529428C>T (hg19) chr1:g.55063755C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063755C>T , CM000663.2:g.55063755C>T GRCh38
NC_000001.10:g.55529428C>T , CM000663.1:g.55529428C>T GRCh37
NC_000001.9:g.55302016C>T NCBI36
NG_009061.1:g.29209C>T , LRG_275:g.29209C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*590C>T ENSP00000501161.2:n.*590C>T
ENST00000710286.1:c.*171C>T ENSP00000518176.1:n.*171C>T
ENST00000673903.1:c.*171C>T ENSP00000501257.1:n.*171C>T
ENST00000302118.5:c.*171C>T MANE Select ENSP00000303208.5:n.*171C>T
ENST00000490692.1:n.2796C>T
NM_174936.3:c.*171C>T , LRG_275t1:c.*171C>T NP_777596.2:n.*171C>T
NR_110451.1:n.1857C>T
XM_011541193.1:c.*171C>T XP_011539495.1:n.*171C>T
NM_174936.4:c.*171C>T MANE Select NP_777596.2:n.*171C>T
NR_110451.2:n.1857C>T
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