Canonical Allele Identifier: CA10602355
Gene:
MyVariant.info:
GRCh38 chr8:g.11564613G>T
GRCh37 chr8:g.11422122G>T
gnomAD v2:
8:11422122 G / T
gnomAD v3:
8:11564613 G / T
gnomAD v4:
chr8-11564613-G-T
Joint Max Group AF 0.00001772 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
Exomes Max Group AF 0.00001651 (NFE)
ClinVar RCV:
RCV000013116
ClinVar Variation:
12323
dbSNP:
886037621
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564613G>T , CM000670.2:g.11564613G>T GRCh38
NC_000008.10:g.11422122G>T , CM000670.1:g.11422122G>T GRCh37
NC_000008.9:g.11459531G>T NCBI36
NG_023543.1:g.75602G>T
NG_023543.2:g.75602G>T
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