Canonical Allele Identifier: CA445498908
Gene: PCSK1 HGNC NCBI

Linked Data

dbSNP Id: rs2112450376
gnomAD v3: 5-96429312-A-C
gnomAD v4: 5-96429312-A-C
MyVariant Identifiers: chr5:g.95765016A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.96429312A>C , CM000667.2:g.96429312A>C GRCh38
NC_000005.9:g.95765016A>C , CM000667.1:g.95765016A>C GRCh37
NC_000005.8:g.95790772A>C NCBI36
NG_021161.1:g.8970T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311106.8:c.186T>G MANE Select ENSP00000308024.2:p.Gly62=
ENST00000311106.7:c.186T>G ENSP00000308024.2:p.Gly62=
ENST00000508626.5:c.45T>G ENSP00000421600.1:p.Gly15=
ENST00000509190.1:c.186T>G ENSP00000427294.1:p.Gly62=
NM_000439.4:c.186T>G NP_000430.3:p.Gly62=
NM_001177875.1:c.45T>G NP_001171346.1:p.Gly15=
NR_130776.1:n.354+49660A>C
NM_000439.5:c.186T>G MANE Select NP_000430.3:p.Gly62=
NM_001177875.2:c.45T>G NP_001171346.1:p.Gly15=