Canonical Allele Identifier: CA340480314
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644758088

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061456G>A , CM000663.2:g.55061456G>A GRCh38
NC_000001.10:g.55527129G>A , CM000663.1:g.55527129G>A GRCh37
NC_000001.9:g.55299717G>A NCBI36
NG_009061.1:g.26910G>A , LRG_275:g.26910G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*103G>A ENSP00000501161.2:n.*103G>A
ENST00000710286.1:c.2120G>A ENSP00000518176.1:p.Cys707Tyr
ENST00000673903.1:c.1388G>A ENSP00000501257.1:p.Cys463Tyr
ENST00000673913.1:c.613G>A ENSP00000501161.1:n.613G>A
ENST00000302118.5:c.1763G>A MANE Select ENSP00000303208.5:p.Cys588Tyr
ENST00000490692.1:n.2309G>A
NM_174936.3:c.1763G>A , LRG_275t1:c.1763G>A NP_777596.2:p.Cys588Tyr
NR_110451.1:n.1370G>A
XM_011541193.1:c.884G>A XP_011539495.1:p.Cys295Tyr
NM_174936.4:c.1763G>A MANE Select NP_777596.2:p.Cys588Tyr
NR_110451.2:n.1370G>A