Canonical Allele Identifier: CA736997997
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1337638608
MyVariant Identifiers: chr1:g.55518779G>A (hg19) chr1:g.55053106G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053106G>A , CM000663.2:g.55053106G>A GRCh38
NC_000001.10:g.55518779G>A , CM000663.1:g.55518779G>A GRCh37
NC_000001.9:g.55291367G>A NCBI36
NG_009061.1:g.18560G>A , LRG_275:g.18560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+315G>A ENSP00000501161.2:n.799+315G>A
ENST00000710286.1:c.1156+315G>A ENSP00000518176.1:n.1156+315G>A
ENST00000673903.1:c.424+315G>A ENSP00000501257.1:n.424+315G>A
ENST00000302118.5:c.799+315G>A MANE Select ENSP00000303208.5:n.799+315G>A
ENST00000490692.1:n.1620+315G>A
NM_174936.3:c.799+315G>A , LRG_275t1:c.799+315G>A NP_777596.2:n.799+315G>A
NR_110451.1:n.458+315G>A
NM_174936.4:c.799+315G>A MANE Select NP_777596.2:n.799+315G>A
NR_110451.2:n.458+315G>A
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