ClinGen Allele Registry
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Canonical Allele Identifier:
CA11957861
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.1392596G>A
GRCh37
chr5:g.1392711G>A
Linked Data - Sequence & Population
gnomAD v2:
5:1392711 G / A
gnomAD v3:
5:1392596 G / A
gnomAD v4:
chr5-1392596-G-A
Joint Max Group AF
0.33629525 (MID)
Genomes Max Group AF
0.25644077 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3863145
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.1392596G>A , CM000667.2:g.1392596G>A
GRCh38
NC_000005.9:g.1392711G>A , CM000667.1:g.1392711G>A
GRCh37
NC_000005.8:g.1445711G>A
NCBI36
NG_015885.1:g.57833C>T
Search 100 bp 5'
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