Canonical Allele Identifier: CA495704312
Gene: CASC16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.52586270T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552358T>A , CM000678.2:g.52552358T>A GRCh38
NC_000016.9:g.52586270T>A , CM000678.1:g.52586270T>A GRCh37
NC_000016.8:g.51143771T>A NCBI36
NG_012623.1:g.445A>T

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.730A>T
Search 100 bp 5'
Search 100 bp 3'