Canonical Allele Identifier: CA495704213
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586253G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552341G>T , CM000678.2:g.52552341G>T GRCh38
NC_000016.9:g.52586253G>T , CM000678.1:g.52586253G>T GRCh37
NC_000016.8:g.51143754G>T NCBI36
NG_012623.1:g.462C>A

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.747C>A