ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11192193
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.97711412A>G
GRCh37
chr2:g.98327875A>G
Linked Data - Sequence & Population
gnomAD v2:
2:98327875 A / G
gnomAD v3:
2:97711412 A / G
gnomAD v4:
chr2-97711412-A-G
Joint Max Group AF
0.24263783 (MID)
Genomes Max Group AF
0.21742409 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17695937
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.97711412A>G , CM000664.2:g.97711412A>G
GRCh38
NC_000002.11:g.98327875A>G , CM000664.1:g.98327875A>G
GRCh37
NC_000002.10:g.97694307A>G
NCBI36
NG_007727.1:g.2845A>G , LRG_126:g.2845A>G
Search 100 bp 5'
Search 100 bp 3'