Canonical Allele Identifier:
CA11831505
Gene:
Linked Data
ClinVar Variation Id:
2571395
ClinVar RCV Id:
RCV003312795
dbSNP Id:
rs4073
gnomAD v2:
4-74606024-A-T
gnomAD v3:
4-73740307-A-T
gnomAD v4:
4-73740307-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73740307A>T , CM000666.2:g.73740307A>T | GRCh38 |
| NC_000004.11:g.74606024A>T , CM000666.1:g.74606024A>T | GRCh37 |
| NC_000004.10:g.74824888A>T | NCBI36 |
| NG_029889.1:g.4802A>T |