Canonical Allele Identifier: CA683048748

Gene: CASC18

Linked Data

• dbSNP Id: rs1421786787
• MyVariant Identifiers: chr12:g.106108972C>T (hg19) ; chr12:g.105715194C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.105715194C>T , CM000674.2:g.105715194C>T	GRCh38
NC_000012.11:g.106108972C>T , CM000674.1:g.106108972C>T	GRCh37
NC_000012.10:g.104633102C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110108.1:n.54+10938C>T
NR_110109.1:n.87C>T
NR_110110.1:n.83+8338C>T
NR_110111.1:n.83+8338C>T
NR_110111.2:n.83+8338C>T