Canonical Allele Identifier: CA14758325
Gene:
MyVariant.info:
GRCh38 chr20:g.46118099C>T
GRCh37 chr20:g.44746738C>T
gnomAD v2:
20:44746738 C / T
gnomAD v3:
20:46118099 C / T
gnomAD v4:
chr20-46118099-C-T
Joint Max Group AF 0.2998081 (SAS)
Genomes Max Group AF 0.2998081 (SAS)
ClinVar RCV:
RCV001710265
ClinVar Variation:
1286483
dbSNP:
752118
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118099C>T , CM000682.2:g.46118099C>T GRCh38
NC_000020.10:g.44746738C>T , CM000682.1:g.44746738C>T GRCh37
NC_000020.9:g.44180145C>T NCBI36
NG_007279.1:g.4833C>T , LRG_40:g.4833C>T
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