Canonical Allele Identifier: CA417957258
Gene: PCSK9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55505549G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039876G>C , CM000663.2:g.55039876G>C GRCh38
NC_000001.10:g.55505549G>C , CM000663.1:g.55505549G>C GRCh37
NC_000001.9:g.55278137G>C NCBI36
NG_009061.1:g.5330G>C , LRG_275:g.5330G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.39G>C ENSP00000501161.2:p.Leu13=
ENST00000710286.1:c.396G>C ENSP00000518176.1:p.Leu132=
ENST00000673726.1:c.39G>C ENSP00000501004.1:p.Leu13=
ENST00000302118.5:c.39G>C MANE Select ENSP00000303208.5:p.Leu13=
NM_174936.3:c.39G>C , LRG_275t1:c.39G>C NP_777596.2:p.Leu13=
NM_174936.4:c.39G>C MANE Select NP_777596.2:p.Leu13=
Search 100 bp 5'
Search 100 bp 3'