Canonical Allele Identifier: CA22768804
Gene: PCSK9 HGNC NCBI

Linked Data

dbSNP Id: rs1014422575
MyVariant Identifiers: chr1:g.55529521T>C (hg19) chr1:g.55063848T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063848T>C , CM000663.2:g.55063848T>C GRCh38
NC_000001.10:g.55529521T>C , CM000663.1:g.55529521T>C GRCh37
NC_000001.9:g.55302109T>C NCBI36
NG_009061.1:g.29302T>C , LRG_275:g.29302T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*683T>C ENSP00000501161.2:n.*683T>C
ENST00000710286.1:c.*264T>C ENSP00000518176.1:n.*264T>C
ENST00000673903.1:c.*264T>C ENSP00000501257.1:n.*264T>C
ENST00000302118.5:c.*264T>C MANE Select ENSP00000303208.5:n.*264T>C
ENST00000490692.1:n.2889T>C
NM_174936.3:c.*264T>C , LRG_275t1:c.*264T>C NP_777596.2:n.*264T>C
NR_110451.1:n.1950T>C
XM_011541193.1:c.*264T>C XP_011539495.1:n.*264T>C
NM_174936.4:c.*264T>C MANE Select NP_777596.2:n.*264T>C
NR_110451.2:n.1950T>C
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