Canonical Allele Identifier: CA11915809
Gene:
MyVariant.info:
GRCh38 chr5:g.1297373C>T
GRCh37 chr5:g.1297488C>T
gnomAD v2:
5:1297488 C / T
gnomAD v3:
5:1297373 C / T
gnomAD v4:
chr5-1297373-C-T
Joint Max Group AF 0.49867565 (SAS)
Genomes Max Group AF 0.49867565 (SAS)
ClinVar RCV:
RCV002515605
ClinVar Variation:
225785
dbSNP:
2736108
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1297373C>T , CM000667.2:g.1297373C>T GRCh38
NC_000005.9:g.1297488C>T , CM000667.1:g.1297488C>T GRCh37
NC_000005.8:g.1350488C>T NCBI36
NG_009265.1:g.2675G>A , LRG_343:g.2675G>A
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