ClinGen Allele Registry
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Canonical Allele Identifier:
CA238787659
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.63154939T>G
GRCh37
chr12:g.63548719T>G
Linked Data - Sequence & Population
gnomAD v2:
12:63548719 T / G
gnomAD v3:
12:63154939 T / G
gnomAD v4:
chr12-63154939-T-G
Joint Max Group AF
0.01237314 (AFR)
Genomes Max Group AF
0.01237314 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7298346
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.63154939T>G , CM000674.2:g.63154939T>G
GRCh38
NC_000012.11:g.63548719T>G , CM000674.1:g.63548719T>G
GRCh37
NC_000012.10:g.61834986T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'