ClinGen Allele Registry
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Canonical Allele Identifier:
CA847191336
Gene: CASC11
HGNC
NCBI
Linked Data
dbSNP Id:
rs1389835493
gnomAD v3:
8-127707562-T-A
gnomAD v4:
8-127707562-T-A
MyVariant Identifiers:
chr8:g.128719807T>A (hg19)
chr8:g.127707562T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127707562T>A , CM000670.2:g.127707562T>A
GRCh38
NC_000008.10:g.128719807T>A , CM000670.1:g.128719807T>A
GRCh37
NC_000008.9:g.128788989T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_117102.1:n.366-4319A>T
Search 100 bp 5'
Search 100 bp 3'