ClinGen Allele Registry
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Canonical Allele Identifier:
CA99343732
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.67198722T>G
GRCh37
chr4:g.68064440T>G
Linked Data - Sequence & Population
gnomAD v2:
4:68064440 T / G
gnomAD v3:
4:67198722 T / G
gnomAD v4:
chr4-67198722-T-G
Joint Max Group AF
0.0005624 (AFR)
Genomes Max Group AF
0.0005624 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10518025
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.67198722T>G , CM000666.2:g.67198722T>G
GRCh38
NC_000004.11:g.68064440T>G , CM000666.1:g.68064440T>G
GRCh37
NC_000004.10:g.67747035T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'