ClinGen Allele Registry
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Canonical Allele Identifier:
CA13566034
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.62429955C>A
GRCh37
chr11:g.62197427C>A
Linked Data - Sequence & Population
gnomAD v2:
11:62197427 C / A
gnomAD v3:
11:62429955 C / A
gnomAD v4:
chr11-62429955-C-A
Joint Max Group AF
0.37372822 (NFE)
Genomes Max Group AF
0.37372822 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2077224
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.62429955C>A , CM000673.2:g.62429955C>A
GRCh38
NC_000011.9:g.62197427C>A , CM000673.1:g.62197427C>A
GRCh37
NC_000011.8:g.61954003C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'