ClinGen Allele Registry
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Canonical Allele Identifier:
CA823638849
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.28553539C>G
GRCh37
chr6:g.28521316C>G
Linked Data - Sequence & Population
gnomAD v3:
6:28553539 C / G
gnomAD v4:
chr6-28553539-C-G
Linked Data - NCBI & NCI
dbSNP:
393414
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.28553539C>G , CM000668.2:g.28553539C>G
GRCh38
NC_000006.11:g.28521316C>G , CM000668.1:g.28521316C>G
GRCh37
NC_000006.10:g.28629295C>G
NCBI36
Search 100 bp 5'
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