Linked Data
dbSNP Id:
rs1665544694
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.108875031G>A , CM000663.2:g.108875031G>A | GRCh38 |
| NC_000001.10:g.109417653G>A , CM000663.1:g.109417653G>A | GRCh37 |
| NC_000001.9:g.109219176G>A | NCBI36 |
| NG_028108.1:g.3051G>A | |
| NG_028108.2:g.4682G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357393.6:c.1-25455C>T | ENSP00000349968.6:n.1-25455C>T | |
| ENST00000357393.5:c.115-25455C>T | ENSP00000349968.5:n.115-25455C>T | |
| XR_001738178.1:n.103+109C>T |