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Canonical Allele Identifier:
CA774666330
Gene: CASC17
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.71112519T>C
GRCh37
chr17:g.69108660T>C
Linked Data - NCBI & NCI
dbSNP:
1314727955
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.71112519T>C , CM000679.2:g.71112519T>C
GRCh38
NC_000017.10:g.69108660T>C , CM000679.1:g.69108660T>C
GRCh37
NC_000017.9:g.66620255T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104152.1:n.218-12901A>G
Search 100 bp 5'
Search 100 bp 3'