Canonical Allele Identifier: CA2060730603
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869983362

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715253A>G , CM000674.2:g.105715253A>G GRCh38
NC_000012.11:g.106109031A>G , CM000674.1:g.106109031A>G GRCh37
NC_000012.10:g.104633161A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10997A>G
NR_110109.1:n.112+34A>G
NR_110110.1:n.83+8397A>G
NR_110111.1:n.83+8397A>G
NR_110111.2:n.83+8397A>G