Canonical Allele Identifier: CA13337234
Gene:
gnomAD v2:
10:104597480 T / C
gnomAD v3:
10:102837723 T / C
gnomAD v4:
chr10-102837723-T-C
Joint Max Group AF 0.24958509 (AMR)
Genomes Max Group AF 0.24958509 (AMR)
ClinVar RCV:
RCV001649637
ClinVar Variation:
1247676
dbSNP:
2486758
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102837723T>C , CM000672.2:g.102837723T>C GRCh38
NC_000010.10:g.104597480T>C , CM000672.1:g.104597480T>C GRCh37
NC_000010.9:g.104587470T>C NCBI36
NG_007955.1:g.4811A>G
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