Canonical Allele Identifier: CA495704295
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586267C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552355C>G , CM000678.2:g.52552355C>G GRCh38
NC_000016.9:g.52586267C>G , CM000678.1:g.52586267C>G GRCh37
NC_000016.8:g.51143768C>G NCBI36
NG_012623.1:g.448G>C

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.733G>C
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