ClinGen Allele Registry
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Canonical Allele Identifier:
CA889792712
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.156882671A>G
GRCh37
chr1:g.156852463A>G
Linked Data - Sequence & Population
gnomAD v3:
1:156882671 A / G
gnomAD v4:
chr1-156882671-A-G
Linked Data - NCBI & NCI
dbSNP:
2768759
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.156882671A>G , CM000663.2:g.156882671A>G
GRCh38
NC_000001.10:g.156852463A>G , CM000663.1:g.156852463A>G
GRCh37
NC_000001.9:g.155119087A>G
NCBI36
NG_007493.1:g.71922A>G , LRG_261:g.71922A>G
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