Canonical Allele Identifier: CA495704378
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586282A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552370A>C , CM000678.2:g.52552370A>C GRCh38
NC_000016.9:g.52586282A>C , CM000678.1:g.52586282A>C GRCh37
NC_000016.8:g.51143783A>C NCBI36
NG_012623.1:g.433T>G

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.718T>G
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Search 100 bp 3'