Canonical Allele Identifier: CA2222745329
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552490T= , CM000678.2:g.52552490T= GRCh38
NC_000016.9:g.52586402T= , CM000678.1:g.52586402T= GRCh37
NC_000016.8:g.51143903T= NCBI36
NG_012623.1:g.313A=

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.654-56A=