Canonical Allele Identifier: CA1167981891
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644688834
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053186G>A , CM000663.2:g.55053186G>A GRCh38
NC_000001.10:g.55518859G>A , CM000663.1:g.55518859G>A GRCh37
NC_000001.9:g.55291447G>A NCBI36
NG_009061.1:g.18640G>A , LRG_275:g.18640G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+395G>A ENSP00000501161.2:n.799+395G>A
ENST00000710286.1:c.1156+395G>A ENSP00000518176.1:n.1156+395G>A
ENST00000673903.1:c.424+395G>A ENSP00000501257.1:n.424+395G>A
ENST00000302118.5:c.799+395G>A MANE Select ENSP00000303208.5:n.799+395G>A
ENST00000490692.1:n.1620+395G>A
NM_174936.3:c.799+395G>A , LRG_275t1:c.799+395G>A NP_777596.2:n.799+395G>A
NR_110451.1:n.458+395G>A
NM_174936.4:c.799+395G>A MANE Select NP_777596.2:n.799+395G>A
NR_110451.2:n.458+395G>A
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