ClinGen Allele Registry
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Canonical Allele Identifier:
CA42602999
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.11897380T>A
GRCh37
chr2:g.12037506T>A
Linked Data - Sequence & Population
gnomAD v2:
2:12037506 T / A
gnomAD v3:
2:11897380 T / A
gnomAD v4:
chr2-11897380-T-A
Joint Max Group AF
0.02218483 (AFR)
Genomes Max Group AF
0.02218483 (AFR)
Linked Data - NCBI & NCI
dbSNP:
375216442
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.11897380T>A , CM000664.2:g.11897380T>A
GRCh38
NC_000002.11:g.12037506T>A , CM000664.1:g.12037506T>A
GRCh37
NC_000002.10:g.11954957T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'