ClinGen Allele Registry
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Canonical Allele Identifier:
CA591903118
Gene:
Linked Data
dbSNP Id:
rs1005506038
gnomAD v2:
10-18428442-A-G
gnomAD v3:
10-18139513-A-G
gnomAD v4:
10-18139513-A-G
MyVariant Identifiers:
chr10:g.18428442A>G (hg19)
chr10:g.18139513A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.18139513A>G , CM000672.2:g.18139513A>G
GRCh38
NC_000010.10:g.18428442A>G , CM000672.1:g.18428442A>G
GRCh37
NC_000010.9:g.18468448A>G
NCBI36
NG_016195.1:g.3837A>G
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