ClinGen Allele Registry
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Canonical Allele Identifier:
CA293056365
Gene: CASC17
HGNC
NCBI
Linked Data
dbSNP Id:
rs549009632
gnomAD v2:
17-69108822-T-TA
gnomAD v3:
17-71112681-T-TA
gnomAD v4:
17-71112681-T-TA
MyVariant Identifiers:
chr17:g.69108822_69108823insA (hg19)
chr17:g.71112681_71112682insA (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.71112687dup , CM000679.2:g.71112687dup
GRCh38
NC_000017.10:g.69108828dup , CM000679.1:g.69108828dup
GRCh37
NC_000017.9:g.66620423dup
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_104152.1:n.218-13064dup
Search 100 bp 5'
Search 100 bp 3'