ClinGen Allele Registry
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Canonical Allele Identifier:
CA15178751
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.68419963C>T
GRCh37
chr2:g.68647095C>T
Linked Data - Sequence & Population
gnomAD v2:
2:68647095 C / T
gnomAD v3:
2:68419963 C / T
gnomAD v4:
chr2-68419963-C-T
Joint Max Group AF
0.87800462 (EAS)
Genomes Max Group AF
0.87800462 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7595037
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.68419963C>T , CM000664.2:g.68419963C>T
GRCh38
NC_000002.11:g.68647095C>T , CM000664.1:g.68647095C>T
GRCh37
NC_000002.10:g.68500599C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'