Canonical Allele Identifier: CA185745363
Gene: CASC8 HGNC NCBI

Linked Data

dbSNP Id: rs562518007
gnomAD v2: 8-128484905-C-T
gnomAD v3: 8-127472660-C-T
gnomAD v4: 8-127472660-C-T
MyVariant Identifiers: chr8:g.128484905C>T (hg19) chr8:g.127472660C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127472660C>T , CM000670.2:g.127472660C>T GRCh38
NC_000008.10:g.128484905C>T , CM000670.1:g.128484905C>T GRCh37
NC_000008.9:g.128554087C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024393.1:n.1041+6423G>A
NR_117100.1:n.1041+6423G>A
Search 100 bp 5'
Search 100 bp 3'