Canonical Allele Identifier: CA495703651
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586154G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552242G>T , CM000678.2:g.52552242G>T GRCh38
NC_000016.9:g.52586154G>T , CM000678.1:g.52586154G>T GRCh37
NC_000016.8:g.51143655G>T NCBI36
NG_012623.1:g.561C>A

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.846C>A