ClinGen Allele Registry
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Canonical Allele Identifier:
CA29034877
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.114697195A>G
GRCh37
chr1:g.115239816A>G
Linked Data - Sequence & Population
gnomAD v2:
1:115239816 A / G
gnomAD v3:
1:114697195 A / G
gnomAD v4:
chr1-114697195-A-G
Joint Max Group AF
0.6058302 (SAS)
Genomes Max Group AF
0.6058302 (SAS)
Linked Data - NCBI & NCI
dbSNP:
926938
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.114697195A>G , CM000663.2:g.114697195A>G
GRCh38
NC_000001.10:g.115239816A>G , CM000663.1:g.115239816A>G
GRCh37
NC_000001.9:g.115041339A>G
NCBI36
NG_008012.1:g.3361T>C
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