Canonical Allele Identifier: CA417960382

Gene: PCSK9

Linked Data

• dbSNP Id: rs1356131564
• gnomAD v2: 1-55525200-T-C
• gnomAD v4: 1-55059527-T-C
• MyVariant Identifiers: chr1:g.55525200T>C (hg19) ; chr1:g.55059527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059527T>C , CM000663.2:g.55059527T>C	GRCh38
NC_000001.10:g.55525200T>C , CM000663.1:g.55525200T>C	GRCh37
NC_000001.9:g.55297788T>C	NCBI36
NG_009061.1:g.24981T>C , LRG_275:g.24981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1545T>C	ENSP00000501161.2:p.Phe515=
ENST00000710286.1:c.1902T>C	ENSP00000518176.1:p.Phe634=
ENST00000673903.1:c.1170T>C	ENSP00000501257.1:p.Phe390=
ENST00000673913.1:c.285T>C	ENSP00000501161.1:p.Phe95=
ENST00000302118.5:c.1545T>C MANE Select	ENSP00000303208.5:p.Phe515=
ENST00000490692.1:n.2227+880T>C
NM_174936.3:c.1545T>C , LRG_275t1:c.1545T>C	NP_777596.2:p.Phe515=
NR_110451.1:n.1152T>C
XM_011541193.1:c.666T>C	XP_011539495.1:p.Phe222=
NM_174936.4:c.1545T>C MANE Select	NP_777596.2:p.Phe515=
NR_110451.2:n.1152T>C