ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14749928
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.10787232G>T
GRCh37
chr20:g.10767880G>T
Linked Data - Sequence & Population
gnomAD v2:
20:10767880 G / T
gnomAD v3:
20:10787232 G / T
gnomAD v4:
chr20-10787232-G-T
Joint Max Group AF
0.28021485 (NFE)
Genomes Max Group AF
0.28021485 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1040923
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.10787232G>T , CM000682.2:g.10787232G>T
GRCh38
NC_000020.10:g.10767880G>T , CM000682.1:g.10767880G>T
GRCh37
NC_000020.9:g.10715880G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'