Canonical Allele Identifier: CA122936120
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs955485282
MyVariant Identifiers: chr5:g.95765190G>C (hg19) chr5:g.96429486G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429486G>C , CM000667.2:g.96429486G>C GRCh38
NC_000005.9:g.95765190G>C , CM000667.1:g.95765190G>C GRCh37
NC_000005.8:g.95790946G>C NCBI36
NG_021161.1:g.8796C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-169C>G MANE Select ENSP00000308024.2:n.181-169C>G
ENST00000311106.7:c.181-169C>G ENSP00000308024.2:n.181-169C>G
ENST00000508626.5:c.40-169C>G ENSP00000421600.1:n.40-169C>G
ENST00000509190.1:c.181-169C>G ENSP00000427294.1:n.181-169C>G
NM_000439.4:c.181-169C>G NP_000430.3:n.181-169C>G
NM_001177875.1:c.40-169C>G NP_001171346.1:n.40-169C>G
NR_130776.1:n.354+49834G>C
NM_000439.5:c.181-169C>G MANE Select NP_000430.3:n.181-169C>G
NM_001177875.2:c.40-169C>G NP_001171346.1:n.40-169C>G
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