Canonical Allele Identifier: CA2060730609
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869983631

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715271T>G , CM000674.2:g.105715271T>G GRCh38
NC_000012.11:g.106109049T>G , CM000674.1:g.106109049T>G GRCh37
NC_000012.10:g.104633179T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11015T>G
NR_110109.1:n.112+52T>G
NR_110110.1:n.83+8415T>G
NR_110111.1:n.83+8415T>G
NR_110111.2:n.83+8415T>G