Canonical Allele Identifier: CA495704316
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586271G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552359G>C , CM000678.2:g.52552359G>C GRCh38
NC_000016.9:g.52586271G>C , CM000678.1:g.52586271G>C GRCh37
NC_000016.8:g.51143772G>C NCBI36
NG_012623.1:g.444C>G

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.729C>G