Canonical Allele Identifier: CA14082374
Gene:
MyVariant.info:
GRCh38 chr15:g.58750164C>A
GRCh37 chr15:g.59042363C>A
gnomAD v2:
15:59042363 C / A
gnomAD v3:
15:58750164 C / A
gnomAD v4:
chr15-58750164-C-A
Joint Max Group AF 0.9136308 (EAS)
Genomes Max Group AF 0.9136308 (EAS)
ClinVar RCV:
RCV001617478
ClinVar Variation:
1233353
dbSNP:
514049
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58750164C>A , CM000677.2:g.58750164C>A GRCh38
NC_000015.9:g.59042363C>A , CM000677.1:g.59042363C>A GRCh37
NC_000015.8:g.56829655C>A NCBI36
NG_033876.1:g.4815G>T
NG_033876.2:g.4544G>T
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