Canonical Allele Identifier: CA495703712
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586165A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552253A>C , CM000678.2:g.52552253A>C GRCh38
NC_000016.9:g.52586165A>C , CM000678.1:g.52586165A>C GRCh37
NC_000016.8:g.51143666A>C NCBI36
NG_012623.1:g.550T>G

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.835T>G
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