ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA306681199
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.22558873C>T
GRCh37
chr19:g.22741675C>T
Linked Data - Sequence & Population
gnomAD v2:
19:22741675 C / T
gnomAD v3:
19:22558873 C / T
gnomAD v4:
chr19-22558873-C-T
Joint Max Group AF
0.59097425 (AFR)
Genomes Max Group AF
0.59097425 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8111998
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.22558873C>T , CM000681.2:g.22558873C>T
GRCh38
NC_000019.9:g.22741675C>T , CM000681.1:g.22741675C>T
GRCh37
NC_000019.8:g.22533515C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'