Canonical Allele Identifier: CA171494208
Gene:
MyVariant.info:
GRCh38 chr8:g.6883416A>C
GRCh37 chr8:g.6740938A>C
gnomAD v3:
8:6883416 A / C
gnomAD v4:
chr8-6883416-A-C
Joint Max Group AF 0.00000801 (AFR)
Genomes Max Group AF 0.00000801 (AFR)
dbSNP:
2738173
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6883416A>C , CM000670.2:g.6883416A>C GRCh38
NC_000008.10:g.6740938A>C , CM000670.1:g.6740938A>C GRCh37
NC_000008.9:g.6728348A>C NCBI36
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