ClinGen Allele Registry
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Canonical Allele Identifier:
CA36339656
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.200393892G>C
GRCh37
chr1:g.200363020G>C
Linked Data - NCBI & NCI
dbSNP:
12084681
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.200393892G>C , CM000663.2:g.200393892G>C
GRCh38
NC_000001.10:g.200363020G>C , CM000663.1:g.200363020G>C
GRCh37
NC_000001.9:g.198629643G>C
NCBI36
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