ClinGen Allele Registry
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Canonical Allele Identifier:
CA11078827
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.112829544A>G
GRCh37
chr2:g.113587121A>G
Linked Data - Sequence & Population
gnomAD v2:
2:113587121 A / G
gnomAD v3:
2:112829544 A / G
gnomAD v4:
chr2-112829544-A-G
Joint Max Group AF
0.91407511 (NFE)
Genomes Max Group AF
0.91407511 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2853550
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.112829544A>G , CM000664.2:g.112829544A>G
GRCh38
NC_000002.11:g.113587121A>G , CM000664.1:g.113587121A>G
GRCh37
NC_000002.10:g.113303592A>G
NCBI36
NG_008851.1:g.12236T>C
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