ClinGen Allele Registry
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Canonical Allele Identifier:
CA224512930
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.73987015G>A
GRCh37
chr11:g.73698060G>A
Linked Data - Sequence & Population
gnomAD v2:
11:73698060 G / A
gnomAD v3:
11:73987015 G / A
gnomAD v4:
chr11-73987015-G-A
Joint Max Group AF
0.00138609 (NFE)
Genomes Max Group AF
0.00138609 (NFE)
Linked Data - NCBI & NCI
dbSNP:
591758
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.73987015G>A , CM000673.2:g.73987015G>A
GRCh38
NC_000011.9:g.73698060G>A , CM000673.1:g.73698060G>A
GRCh37
NC_000011.8:g.73375708G>A
NCBI36
NG_011478.1:g.830C>T
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