Canonical Allele Identifier: CA495704170
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586246C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552334C>A , CM000678.2:g.52552334C>A GRCh38
NC_000016.9:g.52586246C>A , CM000678.1:g.52586246C>A GRCh37
NC_000016.8:g.51143747C>A NCBI36
NG_012623.1:g.469G>T

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.754G>T