ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA191792280
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.26208859G>C
GRCh37
chr9:g.26208857G>C
Linked Data - Sequence & Population
gnomAD v2:
9:26208857 G / C
gnomAD v3:
9:26208859 G / C
gnomAD v4:
chr9-26208859-G-C
Joint Max Group AF
0.09284699 (AMR)
Genomes Max Group AF
0.09284699 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4978053
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.26208859G>C , CM000671.2:g.26208859G>C
GRCh38
NC_000009.11:g.26208857G>C , CM000671.1:g.26208857G>C
GRCh37
NC_000009.10:g.26198857G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'