Canonical Allele Identifier: CA495703694
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1963294063
MyVariant Identifiers: chr16:g.52586162G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552250G>A , CM000678.2:g.52552250G>A GRCh38
NC_000016.9:g.52586162G>A , CM000678.1:g.52586162G>A GRCh37
NC_000016.8:g.51143663G>A NCBI36
NG_012623.1:g.553C>T

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.838C>T
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Search 100 bp 3'