Canonical Allele Identifier: CA2222745054
Gene: CASC16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552361A= , CM000678.2:g.52552361A= GRCh38
NC_000016.9:g.52586273A= , CM000678.1:g.52586273A= GRCh37
NC_000016.8:g.51143774A= NCBI36
NG_012623.1:g.442T=

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.727T=