ClinGen Allele Registry
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Canonical Allele Identifier:
CA590030807
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.105892815G>C
GRCh37
chr9:g.108655096G>C
Linked Data - Sequence & Population
gnomAD v2:
9:108655096 G / C
Linked Data - NCBI & NCI
dbSNP:
4742971
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.105892815G>C , CM000671.2:g.105892815G>C
GRCh38
NC_000009.11:g.108655096G>C , CM000671.1:g.108655096G>C
GRCh37
NC_000009.10:g.107694917G>C
NCBI36
Search 100 bp 5'
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