Canonical Allele Identifier: CA2222613013
Gene: CASC22 HGNC NCBI

Linked Data

dbSNP Id: rs12325489

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.52273164C>A , CM000678.2:g.52273164C>A GRCh38
NC_000016.9:g.52307076C>A , CM000678.1:g.52307076C>A GRCh37
NC_000016.8:g.50864577C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933566.1:n.540C>A
XR_933567.1:n.533C>A
XR_933568.1:n.546C>A
XR_933569.1:n.574C>A
XR_933571.1:n.532C>A
XR_933572.1:n.497C>A
NR_135281.1:n.21-6445C>A
XR_001752183.2:n.784C>A