ClinGen Allele Registry
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Canonical Allele Identifier:
CA12515277
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.95404529C>T
GRCh37
chr7:g.95033841C>T
Linked Data - Sequence & Population
gnomAD v2:
7:95033841 C / T
gnomAD v3:
7:95404529 C / T
gnomAD v4:
chr7-95404529-C-T
Joint Max Group AF
0.34966833 (SAS)
Genomes Max Group AF
0.34966833 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7785846
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.95404529C>T , CM000669.2:g.95404529C>T
GRCh38
NC_000007.13:g.95033841C>T , CM000669.1:g.95033841C>T
GRCh37
NC_000007.12:g.94871777C>T
NCBI36
NG_008725.1:g.35544G>A
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