Canonical Allele Identifier: CA185745380
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1013648058
MyVariant Identifiers: chr8:g.128485011G>T (hg19) chr8:g.127472766G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472766G>T , CM000670.2:g.127472766G>T GRCh38
NC_000008.10:g.128485011G>T , CM000670.1:g.128485011G>T GRCh37
NC_000008.9:g.128554193G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6317C>A
NR_117100.1:n.1041+6317C>A
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