Canonical Allele Identifier: CA122898698
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs578232896
MyVariant Identifiers: chr5:g.95727946G>C (hg19) chr5:g.96392242G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96392242G>C , CM000667.2:g.96392242G>C GRCh38
NC_000005.9:g.95727946G>C , CM000667.1:g.95727946G>C GRCh37
NC_000005.8:g.95753702G>C NCBI36
NG_021161.1:g.46040C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.*759C>G MANE Select ENSP00000308024.2:n.*759C>G
ENST00000311106.7:c.*759C>G ENSP00000308024.2:n.*759C>G
NM_000439.4:c.*759C>G NP_000430.3:n.*759C>G
NM_001177875.1:c.*759C>G NP_001171346.1:n.*759C>G
NR_130776.1:n.354+12590G>C
NM_000439.5:c.*759C>G MANE Select NP_000430.3:n.*759C>G
NM_001177875.2:c.*759C>G NP_001171346.1:n.*759C>G
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