Canonical Allele Identifier: CA2222767646
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1378439242

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567252G>A , CM000678.2:g.52567252G>A GRCh38
NC_000016.9:g.52601164G>A , CM000678.1:g.52601164G>A GRCh37
NC_000016.8:g.51158665G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.605-4390C>T