Canonical Allele Identifier: CA13391088
Gene: ME3-DT HGNC NCBI
MyVariant.info:
GRCh38 chr11:g.86703240A>G
GRCh37 chr11:g.86414282A>G
gnomAD v2:
11:86414282 A / G
gnomAD v3:
11:86703240 A / G
gnomAD v4:
chr11-86703240-A-G
Joint Max Group AF 0.47886257 (AFR)
Genomes Max Group AF 0.47886257 (AFR)
Exomes Max Group AF 0.24626806 (NFE)
dbSNP:
2512987
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.86703240A>G , CM000673.2:g.86703240A>G GRCh38
NC_000011.9:g.86414282A>G , CM000673.1:g.86414282A>G GRCh37
NC_000011.8:g.86091930A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748525.1:n.367+113A>G
XR_001748526.1:n.231+113A>G
XR_001748527.1:n.231+113A>G
XR_001748528.1:n.231+113A>G
XR_002957276.1:n.9581+113A>G
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