Canonical Allele Identifier: CA495703205
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586077G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552165G>A , CM000678.2:g.52552165G>A GRCh38
NC_000016.9:g.52586077G>A , CM000678.1:g.52586077G>A GRCh37
NC_000016.8:g.51143578G>A NCBI36
NG_012623.1:g.638C>T

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.923C>T