ClinGen Allele Registry
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Canonical Allele Identifier:
CA12001005
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.56808481A>G
GRCh37
chr5:g.56104308A>G
Linked Data - Sequence & Population
gnomAD v2:
5:56104308 A / G
gnomAD v3:
5:56808481 A / G
gnomAD v4:
chr5-56808481-A-G
Joint Max Group AF
0.81453758 (NFE)
Genomes Max Group AF
0.81453758 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10461617
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.56808481A>G , CM000667.2:g.56808481A>G
GRCh38
NC_000005.9:g.56104308A>G , CM000667.1:g.56104308A>G
GRCh37
NC_000005.8:g.56140065A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'