Canonical Allele Identifier: CA10611401
Gene: PCSK9 HGNC NCBI

Linked Data

ClinVar Variation Id: 297686
dbSNP Id: rs886046427

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039601T>G , CM000663.2:g.55039601T>G GRCh38
NC_000001.10:g.55505274T>G , CM000663.1:g.55505274T>G GRCh37
NC_000001.9:g.55277862T>G NCBI36
NG_009061.1:g.5055T>G , LRG_275:g.5055T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.-237T>G ENSP00000501161.2:n.-237T>G
ENST00000710286.1:c.121T>G ENSP00000518176.1:p.Ser41Ala
ENST00000673726.1:c.-237T>G ENSP00000501004.1:n.-237T>G
ENST00000302118.5:c.-237T>G MANE Select ENSP00000303208.5:n.-237T>G
NM_174936.3:c.-237T>G , LRG_275t1:c.-237T>G NP_777596.2:n.-237T>G
NM_174936.4:c.-237T>G MANE Select NP_777596.2:n.-237T>G