Canonical Allele Identifier: CA847166760
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1170335388
gnomAD v3: 8-127472741-A-T
gnomAD v4: 8-127472741-A-T
MyVariant Identifiers: chr8:g.128484986A>T (hg19) chr8:g.127472741A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472741A>T , CM000670.2:g.127472741A>T GRCh38
NC_000008.10:g.128484986A>T , CM000670.1:g.128484986A>T GRCh37
NC_000008.9:g.128554168A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+6342T>A
NR_117100.1:n.1041+6342T>A
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