Canonical Allele Identifier: CA2222745077
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552365T= , CM000678.2:g.52552365T= GRCh38
NC_000016.9:g.52586277T= , CM000678.1:g.52586277T= GRCh37
NC_000016.8:g.51143778T= NCBI36
NG_012623.1:g.438A=

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.723A=