ClinGen Allele Registry
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Canonical Allele Identifier:
CA717478870
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr15:g.95789632A>T
GRCh37
chr15:g.96332861A>T
Linked Data - NCBI & NCI
dbSNP:
2567426
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.95789632A>T , CM000677.2:g.95789632A>T
GRCh38
NC_000015.9:g.96332861A>T , CM000677.1:g.96332861A>T
GRCh37
NC_000015.8:g.94133865A>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_932654.1:n.148-35557A>T
Search 100 bp 5'
Search 100 bp 3'