ClinGen Allele Registry
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Canonical Allele Identifier:
CA12760550
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.42681912C>T
GRCh37
chr8:g.42537055C>T
Linked Data - Sequence & Population
gnomAD v2:
8:42537055 C / T
gnomAD v3:
8:42681912 C / T
gnomAD v4:
chr8-42681912-C-T
Joint Max Group AF
0.78662432 (EAS)
Genomes Max Group AF
0.78662432 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7842601
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.42681912C>T , CM000670.2:g.42681912C>T
GRCh38
NC_000008.10:g.42537055C>T , CM000670.1:g.42537055C>T
GRCh37
NC_000008.9:g.42656212C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'