ClinGen Allele Registry
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Canonical Allele Identifier:
CA558630922
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.28340062T>C
GRCh37
chr5:g.28340169T>C
Linked Data - Sequence & Population
gnomAD v2:
5:28340169 T / C
gnomAD v3:
5:28340062 T / C
gnomAD v4:
chr5-28340062-T-C
Linked Data - NCBI & NCI
dbSNP:
1175197704
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.28340062T>C , CM000667.2:g.28340062T>C
GRCh38
NC_000005.9:g.28340169T>C , CM000667.1:g.28340169T>C
GRCh37
NC_000005.8:g.28375926T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'