ClinGen Allele Registry
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Canonical Allele Identifier:
CA715632356
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.74733647C>G
GRCh37
chr15:g.75025988C>G
Linked Data - NCBI & NCI
dbSNP:
4886605
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.74733647C>G , CM000677.2:g.74733647C>G
GRCh38
NC_000015.9:g.75025988C>G , CM000677.1:g.75025988C>G
GRCh37
NC_000015.8:g.72813041C>G
NCBI36
NG_008431.1:g.16106C>G
NG_008431.2:g.16106C>G
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