Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128847812T= , CM000669.2:g.128847812T= | GRCh38 |
| NC_000007.13:g.128487866T= , CM000669.1:g.128487866T= | GRCh37 |
| NC_000007.12:g.128275102T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.4404T= MANE Select | ENSP00000327145.8:p.Asp1468= | |
| ENST00000325888.12:c.4404T= | ENSP00000327145.8:p.Asp1468= | |
| ENST00000346177.6:c.4404T= | ENSP00000344002.6:p.Asp1468= | |
| NM_001127487.2:c.4404T= | NP_001120959.1:p.Asp1468= | |
| NM_001458.5:c.4404T= MANE Select | NP_001449.3:p.Asp1468= |