Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18785808G>C , CM000681.2:g.18785808G>C | GRCh38 |
| NC_000019.9:g.18896618G>C , CM000681.1:g.18896618G>C | GRCh37 |
| NC_000019.8:g.18757618G>C | NCBI36 |
| NG_007070.1:g.10497C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000222271.7:c.1533C>G MANE Select | ENSP00000222271.2:p.Asp511Glu | |
| ENST00000222271.6:c.1533C>G | ENSP00000222271.2:p.Asp511Glu | |
| ENST00000425807.1:c.1374C>G | ENSP00000403792.1:p.Asp458Glu | |
| ENST00000542601.6:c.1434C>G | ENSP00000439156.2:p.Asp478Glu | |
| NM_000095.2:c.1533C>G | NP_000086.2:p.Asp511Glu | |
| NM_000095.3:c.1533C>G MANE Select | NP_000086.2:p.Asp511Glu |