Canonical Allele Identifier: CA742279131
Gene: CST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23633113G>C , CM000682.2:g.23633113G>C GRCh38
NC_000020.10:g.23613750G>C , CM000682.1:g.23613750G>C GRCh37
NC_000020.9:g.23561750G>C NCBI36
NG_012887.2:g.9825C>G
NG_012887.3:g.9825C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000398411.5:c.*2+801C>G ENSP00000381448.1:n.*2+801C>G
NM_001288614.1:c.*2+801C>G NP_001275543.1:n.*2+801C>G
NM_001288614.2:c.*2+801C>G NP_001275543.1:n.*2+801C>G