ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15674301
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.125447269T>C
GRCh37
chr10:g.127135838T>C
Linked Data - Sequence & Population
gnomAD v2:
10:127135838 T / C
gnomAD v3:
10:125447269 T / C
gnomAD v4:
chr10-125447269-T-C
Joint Max Group AF
0.88173659 (EAS)
Genomes Max Group AF
0.88173659 (EAS)
Linked Data - NCBI & NCI
dbSNP:
989507
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.125447269T>C , CM000672.2:g.125447269T>C
GRCh38
NC_000010.10:g.127135838T>C , CM000672.1:g.127135838T>C
GRCh37
NC_000010.9:g.127125828T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'