ClinGen Allele Registry
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Canonical Allele Identifier:
CA16438707
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.21250045T>C
GRCh37
chr12:g.21402979T>C
Linked Data - Sequence & Population
gnomAD v2:
12:21402979 T / C
gnomAD v3:
12:21250045 T / C
gnomAD v4:
chr12-21250045-T-C
Joint Max Group AF
0.44169662 (EAS)
Genomes Max Group AF
0.44169662 (EAS)
Linked Data - NCBI & NCI
dbSNP:
113681054
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.21250045T>C , CM000674.2:g.21250045T>C
GRCh38
NC_000012.11:g.21402979T>C , CM000674.1:g.21402979T>C
GRCh37
NC_000012.10:g.21294246T>C
NCBI36
Search 100 bp 5'
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