Canonical Allele Identifier: CA495703704
Gene: CASC16 HGNC NCBI

Linked Data

gnomAD v4: 16-52552251-G-T
MyVariant Identifiers: chr16:g.52586163G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552251G>T , CM000678.2:g.52552251G>T GRCh38
NC_000016.9:g.52586163G>T , CM000678.1:g.52586163G>T GRCh37
NC_000016.8:g.51143664G>T NCBI36
NG_012623.1:g.552C>A

Transcript Alleles

HGVS Amino-acid change
NR_033920.1:n.837C>A
Search 100 bp 5'
Search 100 bp 3'