ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12601448
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.152690784T>G
GRCh37
chr7:g.152387869T>G
Linked Data - Sequence & Population
gnomAD v2:
7:152387869 T / G
gnomAD v3:
7:152690784 T / G
gnomAD v4:
chr7-152690784-T-G
Joint Max Group AF
0.82940609 (AFR)
Genomes Max Group AF
0.82940609 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10234749
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.152690784T>G , CM000669.2:g.152690784T>G
GRCh38
NC_000007.13:g.152387869T>G , CM000669.1:g.152387869T>G
GRCh37
NC_000007.12:g.152018802T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'