Canonical Allele Identifier: CA122936125
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs1008249192
gnomAD v2: 5-95765205-A-G
gnomAD v3: 5-96429501-A-G
gnomAD v4: 5-96429501-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429501A>G , CM000667.2:g.96429501A>G GRCh38
NC_000005.9:g.95765205A>G , CM000667.1:g.95765205A>G GRCh37
NC_000005.8:g.95790961A>G NCBI36
NG_021161.1:g.8781T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.181-184T>C MANE Select ENSP00000308024.2:n.181-184T>C
ENST00000311106.7:c.181-184T>C ENSP00000308024.2:n.181-184T>C
ENST00000508626.5:c.40-184T>C ENSP00000421600.1:n.40-184T>C
ENST00000509190.1:c.181-184T>C ENSP00000427294.1:n.181-184T>C
NM_000439.4:c.181-184T>C NP_000430.3:n.181-184T>C
NM_001177875.1:c.40-184T>C NP_001171346.1:n.40-184T>C
NR_130776.1:n.354+49849A>G
NM_000439.5:c.181-184T>C MANE Select NP_000430.3:n.181-184T>C
NM_001177875.2:c.40-184T>C NP_001171346.1:n.40-184T>C