Canonical Allele Identifier: CA1167978187
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644617274
gnomAD v4: 1-55044073-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55044073G>T , CM000663.2:g.55044073G>T GRCh38
NC_000001.10:g.55509746G>T , CM000663.1:g.55509746G>T GRCh37
NC_000001.9:g.55282334G>T NCBI36
NG_009061.1:g.9527G>T , LRG_275:g.9527G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.399+39G>T ENSP00000501161.2:n.399+39G>T
ENST00000710286.1:c.756+39G>T ENSP00000518176.1:n.756+39G>T
ENST00000673662.1:n.69+39G>T
ENST00000673726.1:c.399+39G>T ENSP00000501004.1:n.399+39G>T
ENST00000673903.1:c.24+39G>T ENSP00000501257.1:n.24+39G>T
ENST00000302118.5:c.399+39G>T MANE Select ENSP00000303208.5:n.399+39G>T
NM_174936.3:c.399+39G>T , LRG_275t1:c.399+39G>T NP_777596.2:n.399+39G>T
NR_110451.1:n.182+3670G>T
NM_174936.4:c.399+39G>T MANE Select NP_777596.2:n.399+39G>T
NR_110451.2:n.182+3670G>T