Canonical Allele Identifier: CA22767262

Gene: PCSK9

Linked Data

• dbSNP Id: rs758634028
• gnomAD v3: 1-55061635-C-T
• gnomAD v4: 1-55061635-C-T
• MyVariant Identifiers: chr1:g.55527308C>T (hg19) ; chr1:g.55061635C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061635C>T , CM000663.2:g.55061635C>T	GRCh38
NC_000001.10:g.55527308C>T , CM000663.1:g.55527308C>T	GRCh37
NC_000001.9:g.55299896C>T	NCBI36
NG_009061.1:g.27089C>T , LRG_275:g.27089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*203+79C>T	ENSP00000501161.2:n.*203+79C>T
ENST00000710286.1:c.2220+79C>T	ENSP00000518176.1:n.2220+79C>T
ENST00000673903.1:c.1488+79C>T	ENSP00000501257.1:n.1488+79C>T
ENST00000673913.1:c.713+79C>T	ENSP00000501161.1:n.713+79C>T
ENST00000302118.5:c.1863+79C>T MANE Select	ENSP00000303208.5:n.1863+79C>T
ENST00000490692.1:n.2409+79C>T
NM_174936.3:c.1863+79C>T , LRG_275t1:c.1863+79C>T	NP_777596.2:n.1863+79C>T
NR_110451.1:n.1470+79C>T
XM_011541193.1:c.984+79C>T	XP_011539495.1:n.984+79C>T
NM_174936.4:c.1863+79C>T MANE Select	NP_777596.2:n.1863+79C>T
NR_110451.2:n.1470+79C>T