Canonical Allele Identifier: CA607493479
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1260802693
gnomAD v2: 12-106108593-G-A
gnomAD v3: 12-105714815-G-A
gnomAD v4: 12-105714815-G-A
MyVariant Identifiers: chr12:g.106108593G>A (hg19) chr12:g.105714815G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714815G>A , CM000674.2:g.105714815G>A GRCh38
NC_000012.11:g.106108593G>A , CM000674.1:g.106108593G>A GRCh37
NC_000012.10:g.104632723G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110108.1:n.54+10559G>A
NR_110109.1:n.55-347G>A
NR_110110.1:n.83+7959G>A
NR_110111.1:n.83+7959G>A
NR_110111.2:n.83+7959G>A
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