Canonical Allele Identifier: CA281877263
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1027871217
gnomAD v2: 16-52601124-C-T
gnomAD v3: 16-52567212-C-T
gnomAD v4: 16-52567212-C-T
MyVariant Identifiers: chr16:g.52601124C>T (hg19) chr16:g.52567212C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52567212C>T , CM000678.2:g.52567212C>T GRCh38
NC_000016.9:g.52601124C>T , CM000678.1:g.52601124C>T GRCh37
NC_000016.8:g.51158625C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.605-4350G>A
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