Canonical Allele Identifier:
CA10818125
Gene:
Linked Data
ClinVar Variation Id:
1232860
ClinVar RCV Id:
RCV001621208
dbSNP Id:
rs2269648
gnomAD v2:
1-169556050-C-T
gnomAD v3:
1-169586812-C-T
gnomAD v4:
1-169586812-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586812C>T , CM000663.2:g.169586812C>T | GRCh38 |
| NC_000001.10:g.169556050C>T , CM000663.1:g.169556050C>T | GRCh37 |
| NC_000001.9:g.167822674C>T | NCBI36 |
| NG_011806.1:g.4720G>A , LRG_553:g.4720G>A |