Canonical Allele Identifier: CA281875501
Gene: CASC16 HGNC NCBI

Linked Data

dbSNP Id: rs564101787

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52552482C>T , CM000678.2:g.52552482C>T GRCh38
NC_000016.9:g.52586394C>T , CM000678.1:g.52586394C>T GRCh37
NC_000016.8:g.51143895C>T NCBI36
NG_012623.1:g.321G>A

Transcript Alleles

HGVS Amino-acid Change
NR_033920.1:n.654-48G>A