Canonical Allele Identifier: CA495704333
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586274A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552362A>G , CM000678.2:g.52552362A>G GRCh38
NC_000016.9:g.52586274A>G , CM000678.1:g.52586274A>G GRCh37
NC_000016.8:g.51143775A>G NCBI36
NG_012623.1:g.441T>C

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.726T>C