Canonical Allele Identifier: CA417960576
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55061544-C-A
MyVariant Identifiers: chr1:g.55527217C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061544C>A , CM000663.2:g.55061544C>A GRCh38
NC_000001.10:g.55527217C>A , CM000663.1:g.55527217C>A GRCh37
NC_000001.9:g.55299805C>A NCBI36
NG_009061.1:g.26998C>A , LRG_275:g.26998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*191C>A ENSP00000501161.2:n.*191C>A
ENST00000710286.1:c.2208C>A ENSP00000518176.1:p.Ala736=
ENST00000673903.1:c.1476C>A ENSP00000501257.1:p.Ala492=
ENST00000673913.1:c.701C>A ENSP00000501161.1:n.701C>A
ENST00000302118.5:c.1851C>A MANE Select ENSP00000303208.5:p.Ala617=
ENST00000490692.1:n.2397C>A
NM_174936.3:c.1851C>A , LRG_275t1:c.1851C>A NP_777596.2:p.Ala617=
NR_110451.1:n.1458C>A
XM_011541193.1:c.972C>A XP_011539495.1:p.Ala324=
NM_174936.4:c.1851C>A MANE Select NP_777596.2:p.Ala617=
NR_110451.2:n.1458C>A