Canonical Allele Identifier: CA13724322
Gene:
MyVariant.info:
GRCh38 chr12:g.49853685G>A
GRCh37 chr12:g.50247468G>A
gnomAD v2:
12:50247468 G / A
gnomAD v3:
12:49853685 G / A
gnomAD v4:
chr12-49853685-G-A
Joint Max Group AF 0.37736144 (NFE)
Genomes Max Group AF 0.37736144 (NFE)
ClinVar RCV:
RCV001002801
ClinVar Variation:
812170
dbSNP:
7138803
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49853685G>A , CM000674.2:g.49853685G>A GRCh38
NC_000012.11:g.50247468G>A , CM000674.1:g.50247468G>A GRCh37
NC_000012.10:g.48533735G>A NCBI36
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