ClinGen Allele Registry
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Canonical Allele Identifier:
CA11212095
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.236613199C>A
GRCh37
chr2:g.237521842C>A
Linked Data - Sequence & Population
gnomAD v2:
2:237521842 C / A
gnomAD v3:
2:236613199 C / A
gnomAD v4:
chr2-236613199-C-A
Joint Max Group AF
0.59808622 (AFR)
Genomes Max Group AF
0.59808622 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7607316
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.236613199C>A , CM000664.2:g.236613199C>A
GRCh38
NC_000002.11:g.237521842C>A , CM000664.1:g.237521842C>A
GRCh37
NC_000002.10:g.237186581C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'