ClinGen Allele Registry
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Canonical Allele Identifier:
CA100043893
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.74052981G>A
GRCh37
chr4:g.74918698G>A
Linked Data - Sequence & Population
gnomAD v2:
4:74918698 G / A
gnomAD v3:
4:74052981 G / A
gnomAD v4:
chr4-74052981-G-A
Joint Max Group AF
0.98051059 (NFE)
Genomes Max Group AF
0.98051059 (NFE)
Linked Data - NCBI & NCI
dbSNP:
352038
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.74052981G>A , CM000666.2:g.74052981G>A
GRCh38
NC_000004.11:g.74918698G>A , CM000666.1:g.74918698G>A
GRCh37
NC_000004.10:g.75137562G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'