Canonical Allele Identifier: CA1167984922
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059593C= , CM000663.2:g.55059593C= GRCh38
NC_000001.10:g.55525266C= , CM000663.1:g.55525266C= GRCh37
NC_000001.9:g.55297854C= NCBI36
NG_009061.1:g.25047C= , LRG_275:g.25047C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1611C= ENSP00000501161.2:p.His537=
ENST00000710286.1:c.1968C= ENSP00000518176.1:p.His656=
ENST00000673903.1:c.1236C= ENSP00000501257.1:p.His412=
ENST00000673913.1:c.351C= ENSP00000501161.1:p.His117=
ENST00000302118.5:c.1611C= MANE Select ENSP00000303208.5:p.His537=
ENST00000490692.1:n.2227+946C=
NM_174936.3:c.1611C= , LRG_275t1:c.1611C= NP_777596.2:p.His537=
NR_110451.1:n.1218C=
XM_011541193.1:c.732C= XP_011539495.1:p.His244=
NM_174936.4:c.1611C= MANE Select NP_777596.2:p.His537=
NR_110451.2:n.1218C=