Canonical Allele Identifier: CA1167978034
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043703G= , CM000663.2:g.55043703G= GRCh38
NC_000001.10:g.55509376G= , CM000663.1:g.55509376G= GRCh37
NC_000001.9:g.55281964G= NCBI36
NG_009061.1:g.9157G= , LRG_275:g.9157G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.208-140G= ENSP00000501161.2:n.208-140G=
ENST00000710286.1:c.565-140G= ENSP00000518176.1:n.565-140G=
ENST00000673726.1:c.208-140G= ENSP00000501004.1:n.208-140G=
ENST00000673903.1:c.-168-140G= ENSP00000501257.1:n.-168-140G=
ENST00000302118.5:c.208-140G= MANE Select ENSP00000303208.5:n.208-140G=
NM_174936.3:c.208-140G= , LRG_275t1:c.208-140G= NP_777596.2:n.208-140G=
NR_110451.1:n.182+3300G=
NM_174936.4:c.208-140G= MANE Select NP_777596.2:n.208-140G=
NR_110451.2:n.182+3300G=