Canonical Allele Identifier: CA951438615
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869984620
gnomAD v3: 12-105715293-A-C
gnomAD v4: 12-105715293-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105715293A>C , CM000674.2:g.105715293A>C GRCh38
NC_000012.11:g.106109071A>C , CM000674.1:g.106109071A>C GRCh37
NC_000012.10:g.104633201A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+11037A>C
NR_110109.1:n.112+74A>C
NR_110110.1:n.83+8437A>C
NR_110111.1:n.83+8437A>C
NR_110111.2:n.83+8437A>C
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