Canonical Allele Identifier: CA1167981877
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1326323424
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053133G>C , CM000663.2:g.55053133G>C GRCh38
NC_000001.10:g.55518806G>C , CM000663.1:g.55518806G>C GRCh37
NC_000001.9:g.55291394G>C NCBI36
NG_009061.1:g.18587G>C , LRG_275:g.18587G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+342G>C ENSP00000501161.2:n.799+342G>C
ENST00000710286.1:c.1156+342G>C ENSP00000518176.1:n.1156+342G>C
ENST00000673903.1:c.424+342G>C ENSP00000501257.1:n.424+342G>C
ENST00000302118.5:c.799+342G>C MANE Select ENSP00000303208.5:n.799+342G>C
ENST00000490692.1:n.1620+342G>C
NM_174936.3:c.799+342G>C , LRG_275t1:c.799+342G>C NP_777596.2:n.799+342G>C
NR_110451.1:n.458+342G>C
NM_174936.4:c.799+342G>C MANE Select NP_777596.2:n.799+342G>C
NR_110451.2:n.458+342G>C
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