ClinGen Allele Registry
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Canonical Allele Identifier:
CA672159126
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.116793324G>C
GRCh37
chr11:g.116664040G>C
Linked Data - NCBI & NCI
dbSNP:
10750097
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116793324G>C , CM000673.2:g.116793324G>C
GRCh38
NC_000011.9:g.116664040G>C , CM000673.1:g.116664040G>C
GRCh37
NC_000011.8:g.116169250G>C
NCBI36
NG_015894.1:g.4097C>G
NG_015894.2:g.4097C>G
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