Canonical Allele Identifier: CA2726880799
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs2121209527
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715329T>A , CM000674.2:g.105715329T>A GRCh38
NC_000012.11:g.106109107T>A , CM000674.1:g.106109107T>A GRCh37
NC_000012.10:g.104633237T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11073T>A
NR_110109.1:n.112+110T>A
NR_110110.1:n.83+8473T>A
NR_110111.1:n.83+8473T>A
NR_110111.2:n.83+8473T>A
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