Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786036T>C , CM000681.2:g.18786036T>C | GRCh38 |
| NC_000019.9:g.18896846T>C , CM000681.1:g.18896846T>C | GRCh37 |
| NC_000019.8:g.18757846T>C | NCBI36 |
| NG_007070.1:g.10269A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000222271.7:c.1418A>G MANE Select | ENSP00000222271.2:p.Asp473Gly | |
| ENST00000222271.6:c.1418A>G | ENSP00000222271.2:p.Asp473Gly | |
| ENST00000425807.1:c.1259A>G | ENSP00000403792.1:p.Asp420Gly | |
| ENST00000542601.6:c.1319A>G | ENSP00000439156.2:p.Asp440Gly | |
| NM_000095.2:c.1418A>G | NP_000086.2:p.Asp473Gly | |
| NM_000095.3:c.1418A>G MANE Select | NP_000086.2:p.Asp473Gly |