Canonical Allele Identifier: CA2222745098
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552374A= , CM000678.2:g.52552374A= GRCh38
NC_000016.9:g.52586286A= , CM000678.1:g.52586286A= GRCh37
NC_000016.8:g.51143787A= NCBI36
NG_012623.1:g.429T=

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.714T=