Linked Data
dbSNP Id:
rs2138321291
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.39329156C>T , CM000675.2:g.39329156C>T | GRCh38 |
| NC_000013.10:g.39903293C>T , CM000675.1:g.39903293C>T | GRCh37 |
| NC_000013.9:g.38801293C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000648377.1:c.*82+14698G>A | ENSP00000496801.1:n.*82+14698G>A | |
| XR_001749845.1:n.1449+7115G>A |