ClinGen Allele Registry
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Canonical Allele Identifier:
CA10982315
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.22631825T>C
GRCh37
chr1:g.22958318T>C
Linked Data - Sequence & Population
gnomAD v2:
1:22958318 T / C
gnomAD v3:
1:22631825 T / C
gnomAD v4:
chr1-22631825-T-C
Joint Max Group AF
0.37678527 (AFR)
Genomes Max Group AF
0.37678527 (AFR)
Linked Data - NCBI & NCI
dbSNP:
587585
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.22631825T>C , CM000663.2:g.22631825T>C
GRCh38
NC_000001.10:g.22958318T>C , CM000663.1:g.22958318T>C
GRCh37
NC_000001.9:g.22830905T>C
NCBI36
NG_007282.1:g.201T>C , LRG_22:g.201T>C
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