Canonical Allele Identifier: CA10771790
Gene:
MyVariant.info:
GRCh38 chr1:g.59926822C>A
GRCh37 chr1:g.60392494C>A
gnomAD v2:
1:60392494 C / A
gnomAD v3:
1:59926822 C / A
gnomAD v4:
chr1-59926822-C-A
Joint Max Group AF 0.13894687 (AFR)
Genomes Max Group AF 0.13881628 (AFR)
Exomes Max Group AF 0.13678286 (AFR)
dbSNP:
890293
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.59926822C>A , CM000663.2:g.59926822C>A GRCh38
NC_000001.10:g.60392494C>A , CM000663.1:g.60392494C>A GRCh37
NC_000001.9:g.60165082C>A NCBI36
NG_007931.1:g.4930G>T
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