ClinGen Allele Registry
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Canonical Allele Identifier:
CA15736639
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.114914926G>A
GRCh37
chr12:g.115352731G>A
Linked Data - Sequence & Population
gnomAD v2:
12:115352731 G / A
gnomAD v3:
12:114914926 G / A
gnomAD v4:
chr12-114914926-G-A
Joint Max Group AF
0.4088174 (MID)
Genomes Max Group AF
0.34177533 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2384550
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.114914926G>A , CM000674.2:g.114914926G>A
GRCh38
NC_000012.11:g.115352731G>A , CM000674.1:g.115352731G>A
GRCh37
NC_000012.10:g.113837114G>A
NCBI36
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