ClinGen Allele Registry
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Canonical Allele Identifier:
CA106993704
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.136605429T>C
GRCh37
chr4:g.137526584T>C
Linked Data - Sequence & Population
gnomAD v2:
4:137526584 T / C
gnomAD v3:
4:136605429 T / C
gnomAD v4:
chr4-136605429-T-C
Joint Max Group AF
0.49492449 (AFR)
Genomes Max Group AF
0.49492449 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10012307
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.136605429T>C , CM000666.2:g.136605429T>C
GRCh38
NC_000004.11:g.137526584T>C , CM000666.1:g.137526584T>C
GRCh37
NC_000004.10:g.137746034T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'