ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA191256907
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.22133995G>A
GRCh37
chr9:g.22133994G>A
Linked Data - Sequence & Population
gnomAD v3:
9:22133995 G / A
gnomAD v4:
chr9-22133995-G-A
Linked Data - NCBI & NCI
dbSNP:
561730981
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.22133995G>A , CM000671.2:g.22133995G>A
GRCh38
NC_000009.11:g.22133994G>A , CM000671.1:g.22133994G>A
GRCh37
NC_000009.10:g.22123994G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'