ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA211725093
Gene:
Linked Data
dbSNP Id:
rs184939214
gnomAD v2:
10-96697172-T-G
gnomAD v3:
10-94937415-T-G
gnomAD v4:
10-94937415-T-G
MyVariant Identifiers:
chr10:g.96697172T>G (hg19)
chr10:g.96697172_96697173delinsGG (hg19)
chr10:g.94937415T>G (hg38)
chr10:g.94937415_94937416delinsGG (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.94937415T>G , CM000672.2:g.94937415T>G
GRCh38
NC_000010.10:g.96697172T>G , CM000672.1:g.96697172T>G
GRCh37
NC_000010.9:g.96687162T>G
NCBI36
NG_008385.1:g.3758T>G
NG_008385.2:g.4258T>G
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