Linked Data
dbSNP Id:
rs1309887072
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80152744T>G , CM000677.2:g.80152744T>G | GRCh38 |
| NC_000015.9:g.80445086T>G , CM000677.1:g.80445086T>G | GRCh37 |
| NC_000015.8:g.78232141T>G | NCBI36 |
| NG_012833.1:g.4746T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558022.5:c.-30+199T>G | ENSP00000453152.1:n.-30+199T>G |