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Canonical Allele Identifier:
CA185120531
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.121684892C>A
GRCh37
chr8:g.122697132C>A
Linked Data - Sequence & Population
gnomAD v2:
8:122697132 C / A
gnomAD v3:
8:121684892 C / A
gnomAD v4:
chr8-121684892-C-A
Joint Max Group AF
0.77884345 (EAS)
Genomes Max Group AF
0.77884345 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3870371
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.121684892C>A , CM000670.2:g.121684892C>A
GRCh38
NC_000008.10:g.122697132C>A , CM000670.1:g.122697132C>A
GRCh37
NC_000008.9:g.122766313C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'