Canonical Allele Identifier: CA523275579

Gene: PCSK9

Linked Data

• dbSNP Id: rs1200215812
• gnomAD v2: 1-55525363-G-A
• gnomAD v3: 1-55059690-G-A
• gnomAD v4: 1-55059690-G-A
• MyVariant Identifiers: chr1:g.55525363G>A (hg19) ; chr1:g.55059690G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059690G>A , CM000663.2:g.55059690G>A	GRCh38
NC_000001.10:g.55525363G>A , CM000663.1:g.55525363G>A	GRCh37
NC_000001.9:g.55297951G>A	NCBI36
NG_009061.1:g.25144G>A , LRG_275:g.25144G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+27G>A	ENSP00000501161.2:n.1681+27G>A
ENST00000710286.1:c.2038+27G>A	ENSP00000518176.1:n.2038+27G>A
ENST00000673903.1:c.1306+27G>A	ENSP00000501257.1:n.1306+27G>A
ENST00000673913.1:c.421+27G>A	ENSP00000501161.1:n.421+27G>A
ENST00000302118.5:c.1681+27G>A MANE Select	ENSP00000303208.5:n.1681+27G>A
ENST00000490692.1:n.2227+1043G>A
NM_174936.3:c.1681+27G>A , LRG_275t1:c.1681+27G>A	NP_777596.2:n.1681+27G>A
NR_110451.1:n.1288+27G>A
XM_011541193.1:c.802+27G>A	XP_011539495.1:n.802+27G>A
NM_174936.4:c.1681+27G>A MANE Select	NP_777596.2:n.1681+27G>A
NR_110451.2:n.1288+27G>A