Canonical Allele Identifier: CA737022664
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1446198003
MyVariant Identifiers: chr1:g.55505179_55505190del (hg19) chr1:g.55039506_55039517del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039506_55039517del , CM000663.2:g.55039506_55039517del GRCh38
NC_000001.10:g.55505179_55505190del , CM000663.1:g.55505179_55505190del GRCh37
NC_000001.9:g.55277767_55277778del NCBI36
NG_009061.1:g.4960_4971del , LRG_275:g.4960_4971del

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.-332_-321del ENSP00000501161.2:n.-332_-321del
ENST00000710286.1:c.26_37del ENSP00000518176.1:p.Arg9_Val13delinsLeu
ENST00000673726.1:c.-332_-321del ENSP00000501004.1:n.-332_-321del
NM_174936.3:c.-332_-321del , LRG_275t1:c.-332_-321del NP_777596.2:n.-332_-321del
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