Canonical Allele Identifier: CA522961573
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs553095640
gnomAD v2: 1-55529277-G-A
gnomAD v4: 1-55063604-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063604G>A , CM000663.2:g.55063604G>A GRCh38
NC_000001.10:g.55529277G>A , CM000663.1:g.55529277G>A GRCh37
NC_000001.9:g.55301865G>A NCBI36
NG_009061.1:g.29058G>A , LRG_275:g.29058G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*439G>A ENSP00000501161.2:n.*439G>A
ENST00000710286.1:c.*20G>A ENSP00000518176.1:n.*20G>A
ENST00000673903.1:c.*20G>A ENSP00000501257.1:n.*20G>A
ENST00000302118.5:c.*20G>A MANE Select ENSP00000303208.5:n.*20G>A
ENST00000490692.1:n.2645G>A
NM_174936.3:c.*20G>A , LRG_275t1:c.*20G>A NP_777596.2:n.*20G>A
NR_110451.1:n.1706G>A
XM_011541193.1:c.*20G>A XP_011539495.1:n.*20G>A
NM_174936.4:c.*20G>A MANE Select NP_777596.2:n.*20G>A
NR_110451.2:n.1706G>A