Canonical Allele Identifier: CA30986598
Gene:
MyVariant.info:
GRCh38 chr1:g.156060246C>G
gnomAD v3:
1:156060246 C / G
gnomAD v4:
chr1-156060246-C-G
Joint Max Group AF 0.00000488 (NFE)
Genomes Max Group AF 0.00000488 (NFE)
dbSNP:
34372695
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.156060246C>G , CM000663.2:g.156060246C>G GRCh38
NC_000001.10:g.156030037C>G , CM000663.1:g.156030037C>G GRCh37
NC_000001.9:g.154296661C>G NCBI36
NG_009898.1:g.10521C>G , LRG_81:g.10521C>G
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