Canonical Allele Identifier: CA847168633
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1388995667
gnomAD v3: 8-127473850-G-T
gnomAD v4: 8-127473850-G-T
MyVariant Identifiers: chr8:g.128486095G>T (hg19) chr8:g.127473850G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473850G>T , CM000670.2:g.127473850G>T GRCh38
NC_000008.10:g.128486095G>T , CM000670.1:g.128486095G>T GRCh37
NC_000008.9:g.128555277G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5233C>A
NR_117100.1:n.1041+5233C>A
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