Canonical Allele Identifier: CA495703682
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1567363402
MyVariant Identifiers: chr16:g.52586160A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552248A>C , CM000678.2:g.52552248A>C GRCh38
NC_000016.9:g.52586160A>C , CM000678.1:g.52586160A>C GRCh37
NC_000016.8:g.51143661A>C NCBI36
NG_012623.1:g.555T>G

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.840T>G