Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188991519T= , CM000664.2:g.188991519T= | GRCh38 |
| NC_000002.11:g.189856245T= , CM000664.1:g.189856245T= | GRCh37 |
| NC_000002.10:g.189564490T= | NCBI36 |
| NG_007404.1:g.22147T= , LRG_3:g.22147T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000090.4:c.885T= MANE Select | NP_000081.2:p.Ala295= |
| ENST00000304636.9:c.885T= MANE Select | ENSP00000304408.4:p.Ala295= |
| NM_000090.3:c.885T= , LRG_3t1:c.885T= | NP_000081.1:p.Ala295= |
| ENST00000304636.7:c.885T= | ENSP00000304408.3:p.Ala295= |
| ENST00000317840.9:c.885T= | ENSP00000315243.6:p.Ala295= |
| ENST00000450867.2:c.885T= | ENSP00000415346.2:p.Ala295= |