Canonical Allele Identifier: CA418181174
Gene: PCSK9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55518436G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052763G>C , CM000663.2:g.55052763G>C GRCh38
NC_000001.10:g.55518436G>C , CM000663.1:g.55518436G>C GRCh37
NC_000001.9:g.55291024G>C NCBI36
NG_009061.1:g.18217G>C , LRG_275:g.18217G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.771G>C ENSP00000501161.2:p.Gly257=
ENST00000710286.1:c.1128G>C ENSP00000518176.1:p.Gly376=
ENST00000673903.1:c.396G>C ENSP00000501257.1:p.Gly132=
ENST00000302118.5:c.771G>C MANE Select ENSP00000303208.5:p.Gly257=
ENST00000490692.1:n.1592G>C
NM_174936.3:c.771G>C , LRG_275t1:c.771G>C NP_777596.2:p.Gly257=
NR_110451.1:n.430G>C
NM_174936.4:c.771G>C MANE Select NP_777596.2:p.Gly257=
NR_110451.2:n.430G>C
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