ClinGen Allele Registry
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Canonical Allele Identifier:
CA725269565
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.85977731C>G
GRCh37
chr16:g.86011337C>G
Linked Data - NCBI & NCI
dbSNP:
10521318
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.85977731C>G , CM000678.2:g.85977731C>G
GRCh38
NC_000016.9:g.86011337C>G , CM000678.1:g.86011337C>G
GRCh37
NC_000016.8:g.84568838C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'