ClinGen Allele Registry
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Canonical Allele Identifier:
CA63790185
Gene:
Linked Data
dbSNP Id:
rs900436992
MyVariant Identifiers:
chr2:g.204738875A>G (hg19)
chr2:g.203874152A>G (hg38)
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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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