ClinGen Allele Registry
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Canonical Allele Identifier:
CA17996899
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.11728507A>G
GRCh37
chr1:g.11788564A>G
Linked Data - Sequence & Population
gnomAD v2:
1:11788564 A / G
gnomAD v3:
1:11728507 A / G
gnomAD v4:
chr1-11728507-A-G
Joint Max Group AF
0.98206879 (NFE)
Genomes Max Group AF
0.98206879 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4846033
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.11728507A>G , CM000663.2:g.11728507A>G
GRCh38
NC_000001.10:g.11788564A>G , CM000663.1:g.11788564A>G
GRCh37
NC_000001.9:g.11711151A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'