Canonical Allele Identifier: CA340483789
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043984G>C , CM000663.2:g.55043984G>C GRCh38
NC_000001.10:g.55509657G>C , CM000663.1:g.55509657G>C GRCh37
NC_000001.9:g.55282245G>C NCBI36
NG_009061.1:g.9438G>C , LRG_275:g.9438G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.349G>C ENSP00000501161.2:p.Gly117Arg
ENST00000710286.1:c.706G>C ENSP00000518176.1:p.Gly236Arg
ENST00000673662.1:n.19G>C
ENST00000673726.1:c.349G>C ENSP00000501004.1:p.Gly117Arg
ENST00000673903.1:c.-27G>C ENSP00000501257.1:n.-27G>C
ENST00000302118.5:c.349G>C MANE Select ENSP00000303208.5:p.Gly117Arg
NM_174936.3:c.349G>C , LRG_275t1:c.349G>C NP_777596.2:p.Gly117Arg
NR_110451.1:n.182+3581G>C
NM_174936.4:c.349G>C MANE Select NP_777596.2:p.Gly117Arg
NR_110451.2:n.182+3581G>C