Canonical Allele Identifier: CA10770925
Gene:
MyVariant.info:
GRCh38 chr1:g.55030366T>C
GRCh37 chr1:g.55496039T>C
gnomAD v2:
1:55496039 T / C
gnomAD v3:
1:55030366 T / C
gnomAD v4:
chr1-55030366-T-C
Joint Max Group AF 0.17970775 (NFE)
Genomes Max Group AF 0.17970775 (NFE)
ClinVar RCV:
RCV001848595
ClinVar Variation:
1344496
dbSNP:
11206510
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55030366T>C , CM000663.2:g.55030366T>C GRCh38
NC_000001.10:g.55496039T>C , CM000663.1:g.55496039T>C GRCh37
NC_000001.9:g.55268627T>C NCBI36
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