Canonical Allele Identifier: CA495703020
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586045A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552133A>C , CM000678.2:g.52552133A>C GRCh38
NC_000016.9:g.52586045A>C , CM000678.1:g.52586045A>C GRCh37
NC_000016.8:g.51143546A>C NCBI36
NG_012623.1:g.670T>G

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.955T>G