ClinGen Allele Registry
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Canonical Allele Identifier:
CA185773357
Gene: CASC11
HGNC
NCBI
Linked Data
dbSNP Id:
rs1008514426
gnomAD v3:
8-127707677-C-A
gnomAD v4:
8-127707677-C-A
MyVariant Identifiers:
chr8:g.128719922C>A (hg19)
chr8:g.127707677C>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127707677C>A , CM000670.2:g.127707677C>A
GRCh38
NC_000008.10:g.128719922C>A , CM000670.1:g.128719922C>A
GRCh37
NC_000008.9:g.128789104C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_117102.1:n.366-4434G>T
Search 100 bp 5'
Search 100 bp 3'