Canonical Allele Identifier: CA2222767665
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1963449117
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567258C>G , CM000678.2:g.52567258C>G GRCh38
NC_000016.9:g.52601170C>G , CM000678.1:g.52601170C>G GRCh37
NC_000016.8:g.51158671C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.605-4396G>C
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