Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41348385T>G , CM000681.2:g.41348385T>G | GRCh38 |
| NC_000019.9:g.41854290T>G , CM000681.1:g.41854290T>G | GRCh37 |
| NC_000019.8:g.46546130T>G | NCBI36 |
| NG_013364.1:g.10542A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221930.6:c.426A>C MANE Select | ENSP00000221930.4:p.Glu142Asp | |
| ENST00000600196.2:c.426A>C | ENSP00000504008.1:p.Glu142Asp | |
| ENST00000677934.1:c.426A>C | ENSP00000504769.1:p.Glu142Asp | |
| ENST00000221930.5:c.426A>C | ENSP00000221930.4:p.Glu142Asp | |
| NM_000660.5:c.426A>C | NP_000651.3:p.Glu142Asp | |
| XM_011527242.1:c.426A>C | XP_011525544.1:p.Glu142Asp | |
| NM_000660.6:c.426A>C | NP_000651.3:p.Glu142Asp | |
| XM_011527242.2:c.426A>C | XP_011525544.1:p.Glu142Asp | |
| NM_000660.7:c.426A>C MANE Select | NP_000651.3:p.Glu142Asp |