Canonical Allele Identifier: CA522961501

Gene: PCSK9

Linked Data

• dbSNP Id: rs1299308909
• gnomAD v2: 1-55527255-G-A
• MyVariant Identifiers: chr1:g.55527255G>A (hg19) ; chr1:g.55061582G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061582G>A , CM000663.2:g.55061582G>A	GRCh38
NC_000001.10:g.55527255G>A , CM000663.1:g.55527255G>A	GRCh37
NC_000001.9:g.55299843G>A	NCBI36
NG_009061.1:g.27036G>A , LRG_275:g.27036G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*203+26G>A	ENSP00000501161.2:n.*203+26G>A
ENST00000710286.1:c.2220+26G>A	ENSP00000518176.1:n.2220+26G>A
ENST00000673903.1:c.1488+26G>A	ENSP00000501257.1:n.1488+26G>A
ENST00000673913.1:c.713+26G>A	ENSP00000501161.1:n.713+26G>A
ENST00000302118.5:c.1863+26G>A MANE Select	ENSP00000303208.5:n.1863+26G>A
ENST00000490692.1:n.2409+26G>A
NM_174936.3:c.1863+26G>A , LRG_275t1:c.1863+26G>A	NP_777596.2:n.1863+26G>A
NR_110451.1:n.1470+26G>A
XM_011541193.1:c.984+26G>A	XP_011539495.1:n.984+26G>A
NM_174936.4:c.1863+26G>A MANE Select	NP_777596.2:n.1863+26G>A
NR_110451.2:n.1470+26G>A