ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA13370153
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.2179933T>C
GRCh37
chr11:g.2201163T>C
Linked Data - Sequence & Population
gnomAD v2:
11:2201163 T / C
gnomAD v3:
11:2179933 T / C
gnomAD v4:
chr11-2179933-T-C
Joint Max Group AF
0.9080058 (AFR)
Genomes Max Group AF
0.9080058 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6578993
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2179933T>C , CM000673.2:g.2179933T>C
GRCh38
NC_000011.9:g.2201163T>C , CM000673.1:g.2201163T>C
GRCh37
NC_000011.8:g.2157739T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'