Canonical Allele Identifier: CA10581725
Gene:
MyVariant.info:
GRCh38 chr1:g.15438406C>T
GRCh37 chr1:g.15764902C>T
gnomAD v2:
1:15764902 C / T
gnomAD v3:
1:15438406 C / T
gnomAD v4:
chr1-15438406-C-T
Joint Max Group AF 0.0034414 (AMR)
Genomes Max Group AF 0.00442469 (AMR)
Exomes Max Group AF 0.00289631 (AMR)
ClinVar RCV:
RCV000230316
RCV003982975
ClinVar Variation:
240761
dbSNP:
183658182
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15438406C>T , CM000663.2:g.15438406C>T GRCh38
NC_000001.10:g.15764902C>T , CM000663.1:g.15764902C>T GRCh37
NC_000001.9:g.15637489C>T NCBI36
NG_009253.1:g.4965C>T
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