Canonical Allele Identifier: CA15517909
Gene:
MyVariant.info:
GRCh38 chr7:g.9027190C>T
GRCh37 chr7:g.9066820C>T
gnomAD v2:
7:9066820 C / T
gnomAD v3:
7:9027190 C / T
gnomAD v4:
chr7-9027190-C-T
Joint Max Group AF 0.27138885 (AFR)
Genomes Max Group AF 0.27138885 (AFR)
dbSNP:
10952132
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.9027190C>T , CM000669.2:g.9027190C>T GRCh38
NC_000007.13:g.9066820C>T , CM000669.1:g.9066820C>T GRCh37
NC_000007.12:g.9033345C>T NCBI36
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