Canonical Allele Identifier: CA495704322
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586272A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552360A>G , CM000678.2:g.52552360A>G GRCh38
NC_000016.9:g.52586272A>G , CM000678.1:g.52586272A>G GRCh37
NC_000016.8:g.51143773A>G NCBI36
NG_012623.1:g.443T>C

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.728T>C
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