Canonical Allele Identifier: CA951438522
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869975800

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715047C>G , CM000674.2:g.105715047C>G GRCh38
NC_000012.11:g.106108825C>G , CM000674.1:g.106108825C>G GRCh37
NC_000012.10:g.104632955C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10791C>G
NR_110109.1:n.55-115C>G
NR_110110.1:n.83+8191C>G
NR_110111.1:n.83+8191C>G
NR_110111.2:n.83+8191C>G