ClinGen Allele Registry
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Canonical Allele Identifier:
CA159723130
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.56281231A>G
GRCh37
chr7:g.56348924A>G
Linked Data - Sequence & Population
gnomAD v2:
7:56348924 A / G
gnomAD v3:
7:56281231 A / G
gnomAD v4:
chr7-56281231-A-G
Joint Max Group AF
0.24096405 (AMR)
Genomes Max Group AF
0.24096405 (AMR)
Linked Data - NCBI & NCI
dbSNP:
940494
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.56281231A>G , CM000669.2:g.56281231A>G
GRCh38
NC_000007.13:g.56348924A>G , CM000669.1:g.56348924A>G
GRCh37
NC_000007.12:g.56316418A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'