Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204162053C>A , CM000663.2:g.204162053C>A | GRCh38 |
| NC_000001.10:g.204131181C>A , CM000663.1:g.204131181C>A | GRCh37 |
| NC_000001.9:g.202397804C>A | NCBI36 |
| NG_012122.1:g.9285G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.209G>T MANE Select | ENSP00000272190.8:p.Gly70Val | |
| ENST00000638118.1:c.95G>T | ENSP00000490307.1:p.Gly32Val | |
| ENST00000272190.8:c.209G>T | ENSP00000272190.8:p.Gly70Val | |
| NM_000537.3:c.209G>T | NP_000528.1:p.Gly70Val | |
| NM_000537.4:c.209G>T MANE Select | NP_000528.1:p.Gly70Val |