ClinGen Allele Registry
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Canonical Allele Identifier:
CA11078477
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.111191750G>C
GRCh37
chr2:g.111949327G>C
Linked Data - Sequence & Population
gnomAD v2:
2:111949327 G / C
gnomAD v3:
2:111191750 G / C
gnomAD v4:
chr2-111191750-G-C
Joint Max Group AF
0.79877528 (AFR)
Genomes Max Group AF
0.79877528 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6738028
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.111191750G>C , CM000664.2:g.111191750G>C
GRCh38
NC_000002.11:g.111949327G>C , CM000664.1:g.111949327G>C
GRCh37
NC_000002.10:g.111665798G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'