Canonical Allele Identifier: CA2645840780
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55063774-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063774G>C , CM000663.2:g.55063774G>C GRCh38
NC_000001.10:g.55529447G>C , CM000663.1:g.55529447G>C GRCh37
NC_000001.9:g.55302035G>C NCBI36
NG_009061.1:g.29228G>C , LRG_275:g.29228G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*609G>C ENSP00000501161.2:n.*609G>C
ENST00000710286.1:c.*190G>C ENSP00000518176.1:n.*190G>C
ENST00000673903.1:c.*190G>C ENSP00000501257.1:n.*190G>C
ENST00000302118.5:c.*190G>C MANE Select ENSP00000303208.5:n.*190G>C
ENST00000490692.1:n.2815G>C
NM_174936.3:c.*190G>C , LRG_275t1:c.*190G>C NP_777596.2:n.*190G>C
NR_110451.1:n.1876G>C
XM_011541193.1:c.*190G>C XP_011539495.1:n.*190G>C
NM_174936.4:c.*190G>C MANE Select NP_777596.2:n.*190G>C
NR_110451.2:n.1876G>C
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