ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA774666175
Gene: CASC17
HGNC
NCBI
Linked Data
dbSNP Id:
rs1425665954
MyVariant Identifiers:
chr17:g.69108451C>T (hg19)
chr17:g.71112310C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.71112310C>T , CM000679.2:g.71112310C>T
GRCh38
NC_000017.10:g.69108451C>T , CM000679.1:g.69108451C>T
GRCh37
NC_000017.9:g.66620046C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104152.1:n.218-12692G>A
Search 100 bp 5'
Search 100 bp 3'