Canonical Allele Identifier: CA2645840630
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55059358-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059358A>G , CM000663.2:g.55059358A>G GRCh38
NC_000001.10:g.55525031A>G , CM000663.1:g.55525031A>G GRCh37
NC_000001.9:g.55297619A>G NCBI36
NG_009061.1:g.24812A>G , LRG_275:g.24812A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1504-128A>G ENSP00000501161.2:n.1504-128A>G
ENST00000710286.1:c.1861-128A>G ENSP00000518176.1:n.1861-128A>G
ENST00000673903.1:c.1129-128A>G ENSP00000501257.1:n.1129-128A>G
ENST00000673913.1:c.244-128A>G ENSP00000501161.1:n.244-128A>G
ENST00000302118.5:c.1504-128A>G MANE Select ENSP00000303208.5:n.1504-128A>G
ENST00000490692.1:n.2227+711A>G
NM_174936.3:c.1504-128A>G , LRG_275t1:c.1504-128A>G NP_777596.2:n.1504-128A>G
NR_110451.1:n.1111-128A>G
XM_011541193.1:c.625-128A>G XP_011539495.1:n.625-128A>G
NM_174936.4:c.1504-128A>G MANE Select NP_777596.2:n.1504-128A>G
NR_110451.2:n.1111-128A>G