Canonical Allele Identifier: CA495704360
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586279A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552367A>C , CM000678.2:g.52552367A>C GRCh38
NC_000016.9:g.52586279A>C , CM000678.1:g.52586279A>C GRCh37
NC_000016.8:g.51143780A>C NCBI36
NG_012623.1:g.436T>G

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.721T>G