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Canonical Allele Identifier:
CA26370855
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.82589116C>G
GRCh37
chr1:g.83054799C>G
Linked Data - NCBI & NCI
dbSNP:
10874322
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.82589116C>G , CM000663.2:g.82589116C>G
GRCh38
NC_000001.10:g.83054799C>G , CM000663.1:g.83054799C>G
GRCh37
NC_000001.9:g.82827387C>G
NCBI36
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