Canonical Allele Identifier: CA495704338
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586275G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552363G>A , CM000678.2:g.52552363G>A GRCh38
NC_000016.9:g.52586275G>A , CM000678.1:g.52586275G>A GRCh37
NC_000016.8:g.51143776G>A NCBI36
NG_012623.1:g.440C>T

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.725C>T
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Search 100 bp 3'