Canonical Allele Identifier: CA122726
Gene:
MyVariant.info:
GRCh38 chr12:g.88934558T>C
GRCh37 chr12:g.89328335T>C
gnomAD v2:
12:89328335 T / C
gnomAD v3:
12:88934558 T / C
gnomAD v4:
chr12-88934558-T-C
Joint Max Group AF 0.10680613 (NFE)
Genomes Max Group AF 0.10680613 (NFE)
ClinVar RCV:
RCV000013659
ClinVar Variation:
12811
dbSNP:
12821256
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88934558T>C , CM000674.2:g.88934558T>C GRCh38
NC_000012.11:g.89328335T>C , CM000674.1:g.89328335T>C GRCh37
NC_000012.10:g.87852466T>C NCBI36
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