ClinGen Allele Registry
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Canonical Allele Identifier:
CA15332089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.74358873T>C
GRCh37
chr4:g.75224590T>C
Linked Data - Sequence & Population
gnomAD v2:
4:75224590 T / C
gnomAD v3:
4:74358873 T / C
gnomAD v4:
chr4-74358873-T-C
Joint Max Group AF
0.73928633 (NFE)
Genomes Max Group AF
0.73928633 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1350666
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.74358873T>C , CM000666.2:g.74358873T>C
GRCh38
NC_000004.11:g.75224590T>C , CM000666.1:g.75224590T>C
GRCh37
NC_000004.10:g.75443454T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'