Canonical Allele Identifier: CA1167985038

Gene: PCSK9

Linked Data

• dbSNP Id: rs1644746227

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059849C>G , CM000663.2:g.55059849C>G	GRCh38
NC_000001.10:g.55525522C>G , CM000663.1:g.55525522C>G	GRCh37
NC_000001.9:g.55298110C>G	NCBI36
NG_009061.1:g.25303C>G , LRG_275:g.25303C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+186C>G	ENSP00000501161.2:n.1681+186C>G
ENST00000710286.1:c.2038+186C>G	ENSP00000518176.1:n.2038+186C>G
ENST00000673903.1:c.1306+186C>G	ENSP00000501257.1:n.1306+186C>G
ENST00000673913.1:c.421+186C>G	ENSP00000501161.1:n.421+186C>G
ENST00000302118.5:c.1681+186C>G MANE Select	ENSP00000303208.5:n.1681+186C>G
ENST00000490692.1:n.2227+1202C>G
NM_174936.3:c.1681+186C>G , LRG_275t1:c.1681+186C>G	NP_777596.2:n.1681+186C>G
NR_110451.1:n.1288+186C>G
XM_011541193.1:c.802+186C>G	XP_011539495.1:n.802+186C>G
NM_174936.4:c.1681+186C>G MANE Select	NP_777596.2:n.1681+186C>G
NR_110451.2:n.1288+186C>G