Canonical Allele Identifier: CA495704268
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586262C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552350C>T , CM000678.2:g.52552350C>T GRCh38
NC_000016.9:g.52586262C>T , CM000678.1:g.52586262C>T GRCh37
NC_000016.8:g.51143763C>T NCBI36
NG_012623.1:g.453G>A

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.738G>A
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