Canonical Allele Identifier: CA1167981873
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1557504174

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053125G>T , CM000663.2:g.55053125G>T GRCh38
NC_000001.10:g.55518798G>T , CM000663.1:g.55518798G>T GRCh37
NC_000001.9:g.55291386G>T NCBI36
NG_009061.1:g.18579G>T , LRG_275:g.18579G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+334G>T ENSP00000501161.2:n.799+334G>T
ENST00000710286.1:c.1156+334G>T ENSP00000518176.1:n.1156+334G>T
ENST00000673903.1:c.424+334G>T ENSP00000501257.1:n.424+334G>T
ENST00000302118.5:c.799+334G>T MANE Select ENSP00000303208.5:n.799+334G>T
ENST00000490692.1:n.1620+334G>T
NM_174936.3:c.799+334G>T , LRG_275t1:c.799+334G>T NP_777596.2:n.799+334G>T
NR_110451.1:n.458+334G>T
NM_174936.4:c.799+334G>T MANE Select NP_777596.2:n.799+334G>T
NR_110451.2:n.458+334G>T