ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA525281917
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.109279544G>C
GRCh37
chr1:g.109822166G>C
Linked Data - Sequence & Population
gnomAD v2:
1:109822166 G / C
gnomAD v3:
1:109279544 G / C
gnomAD v4:
chr1-109279544-G-C
Joint Max Group AF
0.00001919 (AFR)
Genomes Max Group AF
0.00001919 (AFR)
Linked Data - NCBI & NCI
dbSNP:
599839
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.109279544G>C , CM000663.2:g.109279544G>C
GRCh38
NC_000001.10:g.109822166G>C , CM000663.1:g.109822166G>C
GRCh37
NC_000001.9:g.109623689G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'