Canonical Allele Identifier: CA721497765
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs1280490610
MyVariant Identifiers: chr16:g.52586385A>T (hg19) chr16:g.52552473A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552473A>T , CM000678.2:g.52552473A>T GRCh38
NC_000016.9:g.52586385A>T , CM000678.1:g.52586385A>T GRCh37
NC_000016.8:g.51143886A>T NCBI36
NG_012623.1:g.330T>A

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.654-39T>A
Search 100 bp 5'
Search 100 bp 3'