Canonical Allele Identifier: CA12536266
Gene:
MyVariant.info:
GRCh38 chr7:g.35254361A>G
GRCh37 chr7:g.35293972A>G
gnomAD v2:
7:35293972 A / G
gnomAD v3:
7:35254361 A / G
gnomAD v4:
chr7-35254361-A-G
Joint Max Group AF 0.55248993 (AMR)
Genomes Max Group AF 0.55248993 (AMR)
ClinVar RCV:
RCV001617896
ClinVar Variation:
1235355
dbSNP:
336284
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.35254361A>G , CM000669.2:g.35254361A>G GRCh38
NC_000007.13:g.35293972A>G , CM000669.1:g.35293972A>G GRCh37
NC_000007.12:g.35260497A>G NCBI36
NG_015805.1:g.4740T>C , LRG_755:g.4740T>C
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