Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188994235G= , CM000664.2:g.188994235G= | GRCh38 |
| NC_000002.11:g.189858961G= , CM000664.1:g.189858961G= | GRCh37 |
| NC_000002.10:g.189567206G= | NCBI36 |
| NG_007404.1:g.24863G= , LRG_3:g.24863G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000090.4:c.1196G= MANE Select | NP_000081.2:p.Gly399= |
| ENST00000304636.9:c.1196G= MANE Select | ENSP00000304408.4:p.Gly399= |
| NM_000090.3:c.1196G= , LRG_3t1:c.1196G= | NP_000081.1:p.Gly399= |
| ENST00000304636.7:c.1196G= | ENSP00000304408.3:p.Gly399= |
| ENST00000317840.9:c.1196G= | ENSP00000315243.6:p.Gly399= |
| ENST00000450867.1:c.195G= | |
| ENST00000450867.2:c.1097G= | ENSP00000415346.2:p.Gly366= |