Canonical Allele Identifier: CA11915807
Gene:
MyVariant.info:
GRCh38 chr5:g.1296371A>G
GRCh37 chr5:g.1296486A>G
gnomAD v2:
5:1296486 A / G
gnomAD v3:
5:1296371 A / G
gnomAD v4:
chr5-1296371-A-G
Joint Max Group AF 0.57681971 (AMR)
Genomes Max Group AF 0.57681971 (AMR)
ClinVar RCV:
RCV000498732
RCV001787099
ClinVar Variation:
375479
dbSNP:
2735940
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1296371A>G , CM000667.2:g.1296371A>G GRCh38
NC_000005.9:g.1296486A>G , CM000667.1:g.1296486A>G GRCh37
NC_000005.8:g.1349486A>G NCBI36
NG_009265.1:g.3677T>C , LRG_343:g.3677T>C
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