Canonical Allele Identifier: CA14795530
Gene: PCSK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17455828T>G , CM000682.2:g.17455828T>G GRCh38
NC_000020.10:g.17436473T>G , CM000682.1:g.17436473T>G GRCh37
NC_000020.9:g.17384473T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262545.7:c.1102-520T>G MANE Select ENSP00000262545.2:n.1102-520T>G
ENST00000262545.6:c.1102-520T>G ENSP00000262545.2:n.1102-520T>G
ENST00000377899.5:c.1045-520T>G ENSP00000367131.1:n.1045-520T>G
ENST00000536609.1:c.997-520T>G ENSP00000437458.1:n.997-520T>G
NM_001201528.1:c.1045-520T>G NP_001188457.1:n.1045-520T>G
NM_001201529.2:c.997-520T>G NP_001188458.1:n.997-520T>G
NM_002594.4:c.1102-520T>G NP_002585.2:n.1102-520T>G
NM_002594.5:c.1102-520T>G MANE Select NP_002585.2:n.1102-520T>G
NM_001201529.3:c.997-520T>G NP_001188458.1:n.997-520T>G
NM_001201528.2:c.1045-520T>G NP_001188457.1:n.1045-520T>G
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