Canonical Allele Identifier: CA129034
Gene:
MyVariant.info:
GRCh38 chr11:g.73983709C>T
GRCh37 chr11:g.73694754C>T
gnomAD v2:
11:73694754 C / T
gnomAD v3:
11:73983709 C / T
gnomAD v4:
chr11-73983709-C-T
Joint Max Group AF 0.44762409 (AFR)
Genomes Max Group AF 0.44762409 (AFR)
ClinVar RCV:
RCV000023142
ClinVar Variation:
7865
dbSNP:
659366
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.73983709C>T , CM000673.2:g.73983709C>T GRCh38
NC_000011.9:g.73694754C>T , CM000673.1:g.73694754C>T GRCh37
NC_000011.8:g.73372402C>T NCBI36
NG_011478.1:g.4136G>A
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