Canonical Allele Identifier: CA977368901
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1963448825

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567220G>T , CM000678.2:g.52567220G>T GRCh38
NC_000016.9:g.52601132G>T , CM000678.1:g.52601132G>T GRCh37
NC_000016.8:g.51158633G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.605-4358C>A