ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA44157889
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.22964632C>A
GRCh37
chr2:g.23187504C>A
Linked Data - Sequence & Population
gnomAD v2:
2:23187504 C / A
gnomAD v3:
2:22964632 C / A
gnomAD v4:
chr2-22964632-C-A
Joint Max Group AF
0.71060648 (AFR)
Genomes Max Group AF
0.71060648 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2681019
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.22964632C>A , CM000664.2:g.22964632C>A
GRCh38
NC_000002.11:g.23187504C>A , CM000664.1:g.23187504C>A
GRCh37
NC_000002.10:g.23041009C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'