Canonical Allele Identifier: CA040935

Gene: PCSK9

Linked Data

• ClinVar Variation Id: 921575
• ClinVar RCV Id: RCV001181029 ; RCV001437129 ; RCV002446993
• dbSNP Id: rs779758641
• ExAC: 1:55509542 C / T
• gnomAD v2: 1-55509542-C-T
• gnomAD v3: 1-55043869-C-T
• gnomAD v4: 1-55043869-C-T
• MyVariant Identifiers: chr1:g.55509542C>T (hg19) ; chr1:g.55043869C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55043869C>T , CM000663.2:g.55043869C>T	GRCh38
NC_000001.10:g.55509542C>T , CM000663.1:g.55509542C>T	GRCh37
NC_000001.9:g.55282130C>T	NCBI36
NG_009061.1:g.9323C>T , LRG_275:g.9323C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.234C>T	ENSP00000501161.2:p.Tyr78=
ENST00000710286.1:c.591C>T	ENSP00000518176.1:p.Tyr197=
ENST00000673726.1:c.234C>T	ENSP00000501004.1:p.Tyr78=
ENST00000673903.1:c.-142C>T	ENSP00000501257.1:n.-142C>T
ENST00000302118.5:c.234C>T MANE Select	ENSP00000303208.5:p.Tyr78=
NM_174936.3:c.234C>T , LRG_275t1:c.234C>T	NP_777596.2:p.Tyr78=
NR_110451.1:n.182+3466C>T
NM_174936.4:c.234C>T MANE Select	NP_777596.2:p.Tyr78=
NR_110451.2:n.182+3466C>T