Canonical Allele Identifier: CA12553366
Gene:
MyVariant.info:
GRCh38 chr7:g.1245559A>T
GRCh37 chr7:g.1285195A>T
gnomAD v2:
7:1285195 A / T
gnomAD v3:
7:1245559 A / T
gnomAD v4:
chr7-1245559-A-T
Joint Max Group AF 0.75488523 (NFE)
Genomes Max Group AF 0.75488523 (NFE)
dbSNP:
10277115
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1245559A>T , CM000669.2:g.1245559A>T GRCh38
NC_000007.13:g.1285195A>T , CM000669.1:g.1285195A>T GRCh37
NC_000007.12:g.1251721A>T NCBI36
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