ClinGen Allele Registry
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Canonical Allele Identifier:
CA715979452
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.78622392C>A
GRCh37
chr15:g.78914734C>A
Linked Data - NCBI & NCI
dbSNP:
8023462
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.78622392C>A , CM000677.2:g.78622392C>A
GRCh38
NC_000015.9:g.78914734C>A , CM000677.1:g.78914734C>A
GRCh37
NC_000015.8:g.76701789C>A
NCBI36
NG_016143.1:g.3904G>T
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