ClinGen Allele Registry
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Canonical Allele Identifier:
CA11025141
Gene:
Linked Data
ClinVar Variation Id:
869138
ClinVar RCV Id:
RCV001078162
dbSNP Id:
rs16944
gnomAD v2:
2-113594867-A-G
gnomAD v3:
2-112837290-A-G
gnomAD v4:
2-112837290-A-G
MyVariant Identifiers:
chr2:g.113594867A>G (hg19)
chr2:g.112837290A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.112837290A>G , CM000664.2:g.112837290A>G
GRCh38
NC_000002.11:g.113594867A>G , CM000664.1:g.113594867A>G
GRCh37
NC_000002.10:g.113311338A>G
NCBI36
NG_008851.1:g.4490T>C
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