Canonical Allele Identifier: CA417957297
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55039892-C-T
MyVariant Identifiers: chr1:g.55505565C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039892C>T , CM000663.2:g.55039892C>T GRCh38
NC_000001.10:g.55505565C>T , CM000663.1:g.55505565C>T GRCh37
NC_000001.9:g.55278153C>T NCBI36
NG_009061.1:g.5346C>T , LRG_275:g.5346C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.55C>T ENSP00000501161.2:p.Leu19=
ENST00000710286.1:c.412C>T ENSP00000518176.1:p.Leu138=
ENST00000673726.1:c.55C>T ENSP00000501004.1:p.Leu19=
ENST00000302118.5:c.55C>T MANE Select ENSP00000303208.5:p.Leu19=
NM_174936.3:c.55C>T , LRG_275t1:c.55C>T NP_777596.2:p.Leu19=
NM_174936.4:c.55C>T MANE Select NP_777596.2:p.Leu19=
Search 100 bp 5'
Search 100 bp 3'