Canonical Allele Identifier: CA10889152
Gene:
MyVariant.info:
GRCh38 chr1:g.200966738T>C
GRCh37 chr1:g.200935866T>C
gnomAD v2:
1:200935866 T / C
gnomAD v3:
1:200966738 T / C
gnomAD v4:
chr1-200966738-T-C
Joint Max Group AF 0.29140516 (NFE)
Genomes Max Group AF 0.29136483 (NFE)
Exomes Max Group AF 0.22115648 (NFE)
dbSNP:
11584383
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200966738T>C , CM000663.2:g.200966738T>C GRCh38
NC_000001.10:g.200935866T>C , CM000663.1:g.200935866T>C GRCh37
NC_000001.9:g.199202489T>C NCBI36
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