Canonical Allele Identifier: CA2222744665
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552206A= , CM000678.2:g.52552206A= GRCh38
NC_000016.9:g.52586118A= , CM000678.1:g.52586118A= GRCh37
NC_000016.8:g.51143619A= NCBI36
NG_012623.1:g.597T=

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.882T=