Canonical Allele Identifier: CA1119004559
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs1815899584
gnomAD v3: 8-127473763-T-A
gnomAD v4: 8-127473763-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127473763T>A , CM000670.2:g.127473763T>A GRCh38
NC_000008.10:g.128486008T>A , CM000670.1:g.128486008T>A GRCh37
NC_000008.9:g.128555190T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024393.1:n.1041+5320A>T
NR_117100.1:n.1041+5320A>T
Search 100 bp 5'
Search 100 bp 3'