Canonical Allele Identifier: CA11105634
Gene:
MyVariant.info:
GRCh38 chr2:g.634905T>C
GRCh37 chr2:g.634905T>C
gnomAD v2:
2:634905 T / C
gnomAD v3:
2:634905 T / C
gnomAD v4:
chr2-634905-T-C
Joint Max Group AF 0.8969097 (EAS)
Genomes Max Group AF 0.8969097 (EAS)
ClinVar RCV:
RCV001007461
ClinVar Variation:
812169
dbSNP:
6548238
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.634905T>C , CM000664.2:g.634905T>C GRCh38
NC_000002.11:g.634905T>C , CM000664.1:g.634905T>C GRCh37
NC_000002.10:g.624905T>C NCBI36
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