Canonical Allele Identifier: CA737003380
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1191143013

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059428T>G , CM000663.2:g.55059428T>G GRCh38
NC_000001.10:g.55525101T>G , CM000663.1:g.55525101T>G GRCh37
NC_000001.9:g.55297689T>G NCBI36
NG_009061.1:g.24882T>G , LRG_275:g.24882T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-58T>G ENSP00000501161.2:n.1504-58T>G
ENST00000710286.1:c.1861-58T>G ENSP00000518176.1:n.1861-58T>G
ENST00000673903.1:c.1129-58T>G ENSP00000501257.1:n.1129-58T>G
ENST00000673913.1:c.244-58T>G ENSP00000501161.1:n.244-58T>G
ENST00000302118.5:c.1504-58T>G MANE Select ENSP00000303208.5:n.1504-58T>G
ENST00000490692.1:n.2227+781T>G
NM_174936.3:c.1504-58T>G , LRG_275t1:c.1504-58T>G NP_777596.2:n.1504-58T>G
NR_110451.1:n.1111-58T>G
XM_011541193.1:c.625-58T>G XP_011539495.1:n.625-58T>G
NM_174936.4:c.1504-58T>G MANE Select NP_777596.2:n.1504-58T>G
NR_110451.2:n.1111-58T>G