ClinGen Allele Registry
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Canonical Allele Identifier:
CA105233271
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.122590009T>G
GRCh37
chr4:g.123511164T>G
Linked Data - Sequence & Population
gnomAD v3:
4:122590009 T / G
gnomAD v4:
chr4-122590009-T-G
Joint Max Group AF
0.0000192 (AFR)
Genomes Max Group AF
0.0000192 (AFR)
Linked Data - NCBI & NCI
dbSNP:
906683868
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.122590009T>G , CM000666.2:g.122590009T>G
GRCh38
NC_000004.11:g.123511164T>G , CM000666.1:g.123511164T>G
GRCh37
NC_000004.10:g.123730614T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'