ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10702235
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.218342968G>T
GRCh37
chr1:g.218516310G>T
Linked Data - Sequence & Population
gnomAD v2:
1:218516310 G / T
gnomAD v3:
1:218342968 G / T
gnomAD v4:
chr1-218342968-G-T
Joint Max Group AF
0.64775432 (AFR)
Genomes Max Group AF
0.64775432 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10495098
2100232011
2100232018
2100232024
2100232037
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.218342968G>T , CM000663.2:g.218342968G>T
GRCh38
NC_000001.10:g.218516310G>T , CM000663.1:g.218516310G>T
GRCh37
NC_000001.9:g.216582933G>T
NCBI36
NG_027721.1:g.2635G>T
NG_027721.2:g.2635G>T
Search 100 bp 5'
Search 100 bp 3'