Canonical Allele Identifier: CA13443701
Gene:
MyVariant.info:
GRCh38 chr11:g.67583461G>T
GRCh37 chr11:g.67350932G>T
gnomAD v2:
11:67350932 G / T
gnomAD v3:
11:67583461 G / T
gnomAD v4:
chr11-67583461-G-T
Joint Max Group AF 0.42337718 (NFE)
Genomes Max Group AF 0.42198421 (NFE)
Exomes Max Group AF 0.42219682 (NFE)
ClinVar RCV:
RCV001637500
ClinVar Variation:
1237952
dbSNP:
17593068
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67583461G>T , CM000673.2:g.67583461G>T GRCh38
NC_000011.9:g.67350932G>T , CM000673.1:g.67350932G>T GRCh37
NC_000011.8:g.67107508G>T NCBI36
NG_012075.1:g.4867G>T , LRG_723:g.4867G>T
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