Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154993052T>A , CM000685.2:g.154993052T>A | GRCh38 |
| NC_000023.10:g.154221327T>A , CM000685.1:g.154221327T>A | GRCh37 |
| NC_000023.9:g.153874521T>A | NCBI36 |
| NG_011403.1:g.34672A>T | |
| NG_011403.2:g.34672A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.485A>T MANE Select | ENSP00000353393.4:p.Glu162Val | |
| ENST00000647125.1:c.*271A>T | ENSP00000496062.1:n.*271A>T | |
| ENST00000360256.8:c.485A>T | ENSP00000353393.4:p.Glu162Val | |
| ENST00000423959.5:c.380A>T | ENSP00000409446.1:p.Glu127Val | |
| ENST00000453950.1:c.467A>T | ENSP00000389153.1:p.Glu156Val | |
| NM_000132.3:c.485A>T | NP_000123.1:p.Glu162Val | |
| XM_011531126.1:c.380A>T | XP_011529428.1:p.Glu127Val | |
| NM_000132.4:c.485A>T MANE Select | NP_000123.1:p.Glu162Val |