Linked Data
gnomAD v4:
1-204159489-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204159489T>A , CM000663.2:g.204159489T>A | GRCh38 |
| NC_000001.10:g.204128617T>A , CM000663.1:g.204128617T>A | GRCh37 |
| NC_000001.9:g.202395240T>A | NCBI36 |
| NG_012122.1:g.11849A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272190.9:c.599A>T MANE Select | ENSP00000272190.8:p.Glu200Val | |
| ENST00000638118.1:c.485A>T | ENSP00000490307.1:p.Glu162Val | |
| ENST00000272190.8:c.599A>T | ENSP00000272190.8:p.Glu200Val | |
| NM_000537.3:c.599A>T | NP_000528.1:p.Glu200Val | |
| NM_000537.4:c.599A>T MANE Select | NP_000528.1:p.Glu200Val |