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Canonical Allele Identifier:
CA243959539
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.110976657T>G
GRCh37
chr12:g.111414461T>G
Linked Data - Sequence & Population
gnomAD v2:
12:111414461 T / G
gnomAD v3:
12:110976657 T / G
gnomAD v4:
chr12-110976657-T-G
Joint Max Group AF
0.17705198 (EAS)
Genomes Max Group AF
0.17705198 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12229654
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.110976657T>G , CM000674.2:g.110976657T>G
GRCh38
NC_000012.11:g.111414461T>G , CM000674.1:g.111414461T>G
GRCh37
NC_000012.10:g.109898844T>G
NCBI36
Search 100 bp 5'
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