Canonical Allele Identifier: CA294443541
Gene: CASC17 HGNC NCBI

Linked Data

dbSNP Id: rs967775793
MyVariant Identifiers: chr17:g.69125625T>C (hg19) chr17:g.71129484T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.71129484T>C , CM000679.2:g.71129484T>C GRCh38
NC_000017.10:g.69125625T>C , CM000679.1:g.69125625T>C GRCh37
NC_000017.9:g.66637220T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104152.1:n.217+2906A>G
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