ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15497119
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.100717894A>G
GRCh37
chr7:g.100315517A>G
Linked Data - Sequence & Population
gnomAD v2:
7:100315517 A / G
gnomAD v3:
7:100717894 A / G
gnomAD v4:
chr7-100717894-A-G
Joint Max Group AF
0.91263075 (EAS)
Genomes Max Group AF
0.91263075 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1734907
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.100717894A>G , CM000669.2:g.100717894A>G
GRCh38
NC_000007.13:g.100315517A>G , CM000669.1:g.100315517A>G
GRCh37
NC_000007.12:g.100153453A>G
NCBI36
NG_021471.1:g.2095A>G
NG_021471.2:g.2095A>G
Search 100 bp 5'
Search 100 bp 3'