Canonical Allele Identifier: CA118689
Gene: CTSC HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7297
ClinVar RCV Id: RCV000007720
dbSNP Id: rs104894214

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.88294497C>T , CM000673.2:g.88294497C>T GRCh38
NC_000011.9:g.88027665C>T , CM000673.1:g.88027665C>T GRCh37
NC_000011.8:g.87667313C>T NCBI36
NG_007952.1:g.48277G>A , LRG_50:g.48277G>A

Transcript Alleles

HGVS Amino-acid change
NM_001814.4:c.901G>A , LRG_50t1:c.901G>A NP_001805.3:p.Gly301Ser
NM_001814.5:c.901G>A VV
ENST00000227266.9:c.901G>A ENSP00000227266.4:p.Gly301Ser
ENST00000533897.1:n.3635G>A