Canonical Allele Identifier: CA340474133
Gene: PCSK9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55518428T>A (hg19) chr1:g.55052755T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052755T>A , CM000663.2:g.55052755T>A GRCh38
NC_000001.10:g.55518428T>A , CM000663.1:g.55518428T>A GRCh37
NC_000001.9:g.55291016T>A NCBI36
NG_009061.1:g.18209T>A , LRG_275:g.18209T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.763T>A ENSP00000501161.2:p.Cys255Ser
ENST00000710286.1:c.1120T>A ENSP00000518176.1:p.Cys374Ser
ENST00000673903.1:c.388T>A ENSP00000501257.1:p.Cys130Ser
ENST00000302118.5:c.763T>A MANE Select ENSP00000303208.5:p.Cys255Ser
ENST00000490692.1:n.1584T>A
NM_174936.3:c.763T>A , LRG_275t1:c.763T>A NP_777596.2:p.Cys255Ser
NR_110451.1:n.422T>A
NM_174936.4:c.763T>A MANE Select NP_777596.2:p.Cys255Ser
NR_110451.2:n.422T>A
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