ClinGen Allele Registry
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Canonical Allele Identifier:
CA11262968
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.204263298G>A
GRCh37
chr2:g.205128021G>A
Linked Data - Sequence & Population
gnomAD v2:
2:205128021 G / A
gnomAD v3:
2:204263298 G / A
gnomAD v4:
chr2-204263298-G-A
Joint Max Group AF
0.44596436 (AFR)
Genomes Max Group AF
0.44596436 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6738181
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.204263298G>A , CM000664.2:g.204263298G>A
GRCh38
NC_000002.11:g.205128021G>A , CM000664.1:g.205128021G>A
GRCh37
NC_000002.10:g.204836266G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'