ClinGen Allele Registry
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Canonical Allele Identifier:
CA791553838
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.1783298A>G
GRCh37
chr4:g.1785025A>G
Linked Data - Sequence & Population
gnomAD v3:
4:1783298 A / G
gnomAD v4:
chr4-1783298-A-G
Linked Data - NCBI & NCI
dbSNP:
6599400
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.1783298A>G , CM000666.2:g.1783298A>G
GRCh38
NC_000004.11:g.1785025A>G , CM000666.1:g.1785025A>G
GRCh37
NC_000004.10:g.1754823A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'