Canonical Allele Identifier: CA14851218
Gene:
MyVariant.info:
GRCh38 chr20:g.614136T>C
GRCh37 chr20:g.594780T>C
gnomAD v2:
20:594780 T / C
gnomAD v3:
20:614136 T / C
gnomAD v4:
chr20-614136-T-C
Joint Max Group AF 0.82108945 (EAS)
Genomes Max Group AF 0.82108945 (EAS)
dbSNP:
1533087
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.614136T>C , CM000682.2:g.614136T>C GRCh38
NC_000020.10:g.594780T>C , CM000682.1:g.594780T>C GRCh37
NC_000020.9:g.542780T>C NCBI36
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