Canonical Allele Identifier: CA1167978038
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043717C= , CM000663.2:g.55043717C= GRCh38
NC_000001.10:g.55509390C= , CM000663.1:g.55509390C= GRCh37
NC_000001.9:g.55281978C= NCBI36
NG_009061.1:g.9171C= , LRG_275:g.9171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.208-126C= ENSP00000501161.2:n.208-126C=
ENST00000710286.1:c.565-126C= ENSP00000518176.1:n.565-126C=
ENST00000673726.1:c.208-126C= ENSP00000501004.1:n.208-126C=
ENST00000673903.1:c.-168-126C= ENSP00000501257.1:n.-168-126C=
ENST00000302118.5:c.208-126C= MANE Select ENSP00000303208.5:n.208-126C=
NM_174936.3:c.208-126C= , LRG_275t1:c.208-126C= NP_777596.2:n.208-126C=
NR_110451.1:n.182+3314C=
NM_174936.4:c.208-126C= MANE Select NP_777596.2:n.208-126C=
NR_110451.2:n.182+3314C=
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