Canonical Allele Identifier: CA10657442
Gene:
MyVariant.info:
GRCh38 chr1:g.5294784C>T
GRCh37 chr1:g.5354844C>T
gnomAD v2:
1:5354844 C / T
gnomAD v3:
1:5294784 C / T
gnomAD v4:
chr1-5294784-C-T
Joint Max Group AF 0.38316021 (NFE)
Genomes Max Group AF 0.38316021 (NFE)
dbSNP:
912988
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.5294784C>T , CM000663.2:g.5294784C>T GRCh38
NC_000001.10:g.5354844C>T , CM000663.1:g.5354844C>T GRCh37
NC_000001.9:g.5254704C>T NCBI36
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