Canonical Allele Identifier: CA281877264
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1003302788
MyVariant Identifiers: chr16:g.52601128T>C (hg19) chr16:g.52567216T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567216T>C , CM000678.2:g.52567216T>C GRCh38
NC_000016.9:g.52601128T>C , CM000678.1:g.52601128T>C GRCh37
NC_000016.8:g.51158629T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.605-4354A>G
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