ClinGen Allele Registry
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Canonical Allele Identifier:
CA581027497
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.31638065C>A
GRCh37
chr8:g.31495581C>A
Linked Data - Sequence & Population
gnomAD v2:
8:31495581 C / A
gnomAD v3:
8:31638065 C / A
gnomAD v4:
chr8-31638065-C-A
Linked Data - NCBI & NCI
dbSNP:
6994992
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.31638065C>A , CM000670.2:g.31638065C>A
GRCh38
NC_000008.10:g.31495581C>A , CM000670.1:g.31495581C>A
GRCh37
NC_000008.9:g.31615123C>A
NCBI36
NG_012005.1:g.3314C>A
NG_012005.2:g.3844C>A
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