ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA207736500
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.55657201C>T
GRCh37
chr10:g.57416961C>T
Linked Data - Sequence & Population
gnomAD v2:
10:57416961 C / T
gnomAD v3:
10:55657201 C / T
gnomAD v4:
chr10-55657201-C-T
Joint Max Group AF
0.40227559 (EAS)
Genomes Max Group AF
0.40227559 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1916521
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.55657201C>T , CM000672.2:g.55657201C>T
GRCh38
NC_000010.10:g.57416961C>T , CM000672.1:g.57416961C>T
GRCh37
NC_000010.9:g.57086967C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'