Canonical Allele Identifier: CA12780435
Gene:
MyVariant.info:
GRCh38 chr8:g.142918184A>G
GRCh37 chr8:g.143999600A>G
gnomAD v2:
8:143999600 A / G
gnomAD v3:
8:142918184 A / G
gnomAD v4:
chr8-142918184-A-G
Joint Max Group AF 0.44805314 (NFE)
Genomes Max Group AF 0.44805314 (NFE)
ClinVar RCV:
RCV000937219
ClinVar Variation:
759405
dbSNP:
1799998
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142918184A>G , CM000670.2:g.142918184A>G GRCh38
NC_000008.10:g.143999600A>G , CM000670.1:g.143999600A>G GRCh37
NC_000008.9:g.143996602A>G NCBI36
NG_008374.1:g.4660T>C
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