Linked Data
MyVariant Identifiers:
chr7:g.128485284C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128845230C>T , CM000669.2:g.128845230C>T | GRCh38 |
| NC_000007.13:g.128485284C>T , CM000669.1:g.128485284C>T | GRCh37 |
| NC_000007.12:g.128272520C>T | NCBI36 |
| NG_011807.1:g.19802C>T , LRG_870:g.19802C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.3765C>T MANE Select | ENSP00000327145.8:p.Val1255= | |
| ENST00000325888.12:c.3765C>T | ENSP00000327145.8:p.Val1255= | |
| ENST00000346177.6:c.3765C>T | ENSP00000344002.6:p.Val1255= | |
| NM_001127487.1:c.3765C>T | NP_001120959.1:p.Val1255= | |
| NM_001458.4:c.3765C>T , LRG_870t1:c.3765C>T | NP_001449.3:p.Val1255= | |
| NM_001127487.2:c.3765C>T | NP_001120959.1:p.Val1255= | |
| NM_001458.5:c.3765C>T MANE Select | NP_001449.3:p.Val1255= |