Canonical Allele Identifier: CA2222767632
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567227G= , CM000678.2:g.52567227G= GRCh38
NC_000016.9:g.52601139G= , CM000678.1:g.52601139G= GRCh37
NC_000016.8:g.51158640G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.605-4365C=