ClinGen Allele Registry
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Canonical Allele Identifier:
CA14903370
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr21:g.41616809T>G
GRCh37
chr21:g.43036969T>G
Linked Data - Sequence & Population
gnomAD v2:
21:43036969 T / G
gnomAD v3:
21:41616809 T / G
gnomAD v4:
chr21-41616809-T-G
Joint Max Group AF
0.2790045 (NFE)
Genomes Max Group AF
0.2790045 (NFE)
Linked Data - NCBI & NCI
dbSNP:
9977018
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.41616809T>G , CM000683.2:g.41616809T>G
GRCh38
NC_000021.8:g.43036969T>G , CM000683.1:g.43036969T>G
GRCh37
NC_000021.7:g.41910038T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'