ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA10739229
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.152461533T>G
GRCh37
chr1:g.152434009T>G
Linked Data - Sequence & Population
gnomAD v2:
1:152434009 T / G
gnomAD v3:
1:152461533 T / G
gnomAD v4:
chr1-152461533-T-G
Joint Max Group AF
0.5997175 (EAS)
Genomes Max Group AF
0.5997175 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6700998
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.152461533T>G , CM000663.2:g.152461533T>G
GRCh38
NC_000001.10:g.152434009T>G , CM000663.1:g.152434009T>G
GRCh37
NC_000001.9:g.150700633T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'