Canonical Allele Identifier: CA1001923586
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1644781495
gnomAD v3: 1-55063833-C-T
gnomAD v4: 1-55063833-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063833C>T , CM000663.2:g.55063833C>T GRCh38
NC_000001.10:g.55529506C>T , CM000663.1:g.55529506C>T GRCh37
NC_000001.9:g.55302094C>T NCBI36
NG_009061.1:g.29287C>T , LRG_275:g.29287C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*668C>T ENSP00000501161.2:n.*668C>T
ENST00000710286.1:c.*249C>T ENSP00000518176.1:n.*249C>T
ENST00000673903.1:c.*249C>T ENSP00000501257.1:n.*249C>T
ENST00000302118.5:c.*249C>T MANE Select ENSP00000303208.5:n.*249C>T
ENST00000490692.1:n.2874C>T
NM_174936.3:c.*249C>T , LRG_275t1:c.*249C>T NP_777596.2:n.*249C>T
NR_110451.1:n.1935C>T
XM_011541193.1:c.*249C>T XP_011539495.1:n.*249C>T
NM_174936.4:c.*249C>T MANE Select NP_777596.2:n.*249C>T
NR_110451.2:n.1935C>T