ClinGen Allele Registry
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Canonical Allele Identifier:
CA19759163
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.26148347C>G
GRCh37
chr1:g.26474838C>G
Linked Data - Sequence & Population
gnomAD v2:
1:26474838 C / G
gnomAD v3:
1:26148347 C / G
gnomAD v4:
chr1-26148347-C-G
Joint Max Group AF
0.05629184 (AFR)
Genomes Max Group AF
0.05629184 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7543418
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.26148347C>G , CM000663.2:g.26148347C>G
GRCh38
NC_000001.10:g.26474838C>G , CM000663.1:g.26474838C>G
GRCh37
NC_000001.9:g.26347425C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'