Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67053874C>T , CM000663.2:g.67053874C>T | GRCh38 |
| NC_000001.10:g.67519557C>T , CM000663.1:g.67519557C>T | GRCh37 |
| NC_000001.9:g.67292145C>T | NCBI36 |
| NG_012933.1:g.5524G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235345.6:c.140G>A MANE Select | ENSP00000235345.5:p.Gly47Asp | |
| ENST00000235345.5:c.140G>A | ENSP00000235345.5:p.Gly47Asp | |
| NM_015139.2:c.140G>A | NP_055954.1:p.Gly47Asp | |
| XM_006710478.1:c.140G>A | XP_006710541.1:p.Gly47Asp | |
| XM_011541070.1:c.140G>A | XP_011539372.1:p.Gly47Asp | |
| XM_006710478.2:c.140G>A | XP_006710541.1:p.Gly47Asp | |
| XM_011541070.2:c.140G>A | XP_011539372.1:p.Gly47Asp | |
| XR_001737057.2:n.550G>A | ||
| XR_001737058.2:n.543G>A | ||
| NM_015139.3:c.140G>A MANE Select | NP_055954.1:p.Gly47Asp |