Canonical Allele Identifier: CA737005488

Gene: PCSK9

Linked Data

• dbSNP Id: rs1159560008
• gnomAD v3: 1-55061675-A-G
• gnomAD v4: 1-55061675-A-G
• MyVariant Identifiers: chr1:g.55527348A>G (hg19) ; chr1:g.55061675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061675A>G , CM000663.2:g.55061675A>G	GRCh38
NC_000001.10:g.55527348A>G , CM000663.1:g.55527348A>G	GRCh37
NC_000001.9:g.55299936A>G	NCBI36
NG_009061.1:g.27129A>G , LRG_275:g.27129A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*203+119A>G	ENSP00000501161.2:n.*203+119A>G
ENST00000710286.1:c.2220+119A>G	ENSP00000518176.1:n.2220+119A>G
ENST00000673903.1:c.1488+119A>G	ENSP00000501257.1:n.1488+119A>G
ENST00000673913.1:c.713+119A>G	ENSP00000501161.1:n.713+119A>G
ENST00000302118.5:c.1863+119A>G MANE Select	ENSP00000303208.5:n.1863+119A>G
ENST00000490692.1:n.2409+119A>G
NM_174936.3:c.1863+119A>G , LRG_275t1:c.1863+119A>G	NP_777596.2:n.1863+119A>G
NR_110451.1:n.1470+119A>G
XM_011541193.1:c.984+119A>G	XP_011539495.1:n.984+119A>G
NM_174936.4:c.1863+119A>G MANE Select	NP_777596.2:n.1863+119A>G
NR_110451.2:n.1470+119A>G