ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA777880292
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.25677222T>G
GRCh37
chr18:g.23257186T>G
Linked Data - Sequence & Population
gnomAD v3:
18:25677222 T / G
gnomAD v4:
chr18-25677222-T-G
Linked Data - NCBI & NCI
dbSNP:
1840440
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.25677222T>G , CM000680.2:g.25677222T>G
GRCh38
NC_000018.9:g.23257186T>G , CM000680.1:g.23257186T>G
GRCh37
NC_000018.8:g.21511184T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'