Canonical Allele Identifier: CA2645843042
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55061703-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061703G>C , CM000663.2:g.55061703G>C GRCh38
NC_000001.10:g.55527376G>C , CM000663.1:g.55527376G>C GRCh37
NC_000001.9:g.55299964G>C NCBI36
NG_009061.1:g.27157G>C , LRG_275:g.27157G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+147G>C ENSP00000501161.2:n.*203+147G>C
ENST00000710286.1:c.2220+147G>C ENSP00000518176.1:n.2220+147G>C
ENST00000673903.1:c.1488+147G>C ENSP00000501257.1:n.1488+147G>C
ENST00000673913.1:c.713+147G>C ENSP00000501161.1:n.713+147G>C
ENST00000302118.5:c.1863+147G>C MANE Select ENSP00000303208.5:n.1863+147G>C
ENST00000490692.1:n.2409+147G>C
NM_174936.3:c.1863+147G>C , LRG_275t1:c.1863+147G>C NP_777596.2:n.1863+147G>C
NR_110451.1:n.1470+147G>C
XM_011541193.1:c.984+147G>C XP_011539495.1:n.984+147G>C
NM_174936.4:c.1863+147G>C MANE Select NP_777596.2:n.1863+147G>C
NR_110451.2:n.1470+147G>C