Canonical Allele Identifier: CA14751668
Gene: PCSK2 HGNC NCBI

Linked Data

dbSNP Id: rs6080699

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.17453641G>C , CM000682.2:g.17453641G>C GRCh38
NC_000020.10:g.17434286G>C , CM000682.1:g.17434286G>C GRCh37
NC_000020.9:g.17382286G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262545.7:c.886-101G>C MANE Select ENSP00000262545.2:n.886-101G>C
ENST00000262545.6:c.886-101G>C ENSP00000262545.2:n.886-101G>C
ENST00000377899.5:c.829-101G>C ENSP00000367131.1:n.829-101G>C
ENST00000536609.1:c.781-101G>C ENSP00000437458.1:n.781-101G>C
NM_001201528.1:c.829-101G>C NP_001188457.1:n.829-101G>C
NM_001201529.2:c.781-101G>C NP_001188458.1:n.781-101G>C
NM_002594.4:c.886-101G>C NP_002585.2:n.886-101G>C
NM_002594.5:c.886-101G>C MANE Select NP_002585.2:n.886-101G>C
NM_001201529.3:c.781-101G>C NP_001188458.1:n.781-101G>C
NM_001201528.2:c.829-101G>C NP_001188457.1:n.829-101G>C