ClinGen Allele Registry
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Canonical Allele Identifier:
CA746624745
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.6787030C>A
GRCh37
chr20:g.6767677C>A
Linked Data - Sequence & Population
gnomAD v3:
20:6787030 C / A
gnomAD v4:
chr20-6787030-C-A
Linked Data - NCBI & NCI
dbSNP:
235754
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.6787030C>A , CM000682.2:g.6787030C>A
GRCh38
NC_000020.10:g.6767677C>A , CM000682.1:g.6767677C>A
GRCh37
NC_000020.9:g.6715677C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'