Canonical Allele Identifier: CA15885096
Gene: CASC22 HGNC NCBI

Linked Data

dbSNP Id: rs12325489

Genomic Alleles

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

Transcript Alleles

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