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Canonical Allele Identifier:
CA63790185
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874152A>G
GRCh37
chr2:g.204738875A>G
Linked Data - NCBI & NCI
dbSNP:
900436992
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874152A>G , CM000664.2:g.203874152A>G
GRCh38
NC_000002.11:g.204738875A>G , CM000664.1:g.204738875A>G
GRCh37
NC_000002.10:g.204447120A>G
NCBI36
NG_011502.1:g.11367A>G
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