Linked Data
dbSNP Id:
rs2106662722
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.59705534T>C , CM000665.2:g.59705534T>C | GRCh38 |
| NC_000003.11:g.59691260T>C , CM000665.1:g.59691260T>C | GRCh37 |
| NC_000003.10:g.59666300T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_002959675.1:n.1218-104198T>C |