Canonical Allele Identifier: CA737002187
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1160873547

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55058451G>T , CM000663.2:g.55058451G>T GRCh38
NC_000001.10:g.55524124G>T , CM000663.1:g.55524124G>T GRCh37
NC_000001.9:g.55296712G>T NCBI36
NG_009061.1:g.23905G>T , LRG_275:g.23905G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1355-48G>T ENSP00000501161.2:n.1355-48G>T
ENST00000710286.1:c.1712-48G>T ENSP00000518176.1:n.1712-48G>T
ENST00000673903.1:c.980-48G>T ENSP00000501257.1:n.980-48G>T
ENST00000673913.1:c.95-48G>T ENSP00000501161.1:n.95-48G>T
ENST00000302118.5:c.1355-48G>T MANE Select ENSP00000303208.5:n.1355-48G>T
ENST00000490692.1:n.2079-48G>T
NM_174936.3:c.1355-48G>T , LRG_275t1:c.1355-48G>T NP_777596.2:n.1355-48G>T
NR_110451.1:n.962-48G>T
XM_011541193.1:c.476-48G>T XP_011539495.1:n.476-48G>T
NM_174936.4:c.1355-48G>T MANE Select NP_777596.2:n.1355-48G>T
NR_110451.2:n.962-48G>T