Canonical Allele Identifier: CA15966373
Gene: CST3 HGNC NCBI

Linked Data

dbSNP Id: rs13038305

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23629625C>T , CM000682.2:g.23629625C>T GRCh38
NC_000020.10:g.23610262C>T , CM000682.1:g.23610262C>T GRCh37
NC_000020.9:g.23558262C>T NCBI36
NG_012887.2:g.13313G>A
NG_012887.3:g.13313G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000398411.5:c.*3-160G>A ENSP00000381448.1:n.*3-160G>A
NM_001288614.1:c.*3-160G>A NP_001275543.1:n.*3-160G>A
NM_001288614.2:c.*3-160G>A NP_001275543.1:n.*3-160G>A