Canonical Allele Identifier: CA495703589
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586142T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552230T>G , CM000678.2:g.52552230T>G GRCh38
NC_000016.9:g.52586142T>G , CM000678.1:g.52586142T>G GRCh37
NC_000016.8:g.51143643T>G NCBI36
NG_012623.1:g.573A>C

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.858A>C
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