Canonical Allele Identifier: CA2645843052
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55061706-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061706G>T , CM000663.2:g.55061706G>T GRCh38
NC_000001.10:g.55527379G>T , CM000663.1:g.55527379G>T GRCh37
NC_000001.9:g.55299967G>T NCBI36
NG_009061.1:g.27160G>T , LRG_275:g.27160G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+150G>T ENSP00000501161.2:n.*203+150G>T
ENST00000710286.1:c.2220+150G>T ENSP00000518176.1:n.2220+150G>T
ENST00000673903.1:c.1488+150G>T ENSP00000501257.1:n.1488+150G>T
ENST00000673913.1:c.713+150G>T ENSP00000501161.1:n.713+150G>T
ENST00000302118.5:c.1863+150G>T MANE Select ENSP00000303208.5:n.1863+150G>T
ENST00000490692.1:n.2409+150G>T
NM_174936.3:c.1863+150G>T , LRG_275t1:c.1863+150G>T NP_777596.2:n.1863+150G>T
NR_110451.1:n.1470+150G>T
XM_011541193.1:c.984+150G>T XP_011539495.1:n.984+150G>T
NM_174936.4:c.1863+150G>T MANE Select NP_777596.2:n.1863+150G>T
NR_110451.2:n.1470+150G>T