Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124257T= , CM000664.2:g.71124257T= | GRCh38 |
| NC_000002.11:g.71351387T= , CM000664.1:g.71351387T= | GRCh37 |
| NC_000002.10:g.71204895T= | NCBI36 |
| NG_008977.1:g.11008A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.327A= MANE Select | ENSP00000244217.5:p.Ala109= | |
| ENST00000244217.5:c.327A= | ENSP00000244217.5:p.Ala109= | |
| ENST00000413592.5:c.84+111A= | ENSP00000391140.1:n.84+111A= | |
| ENST00000486135.1:c.42A= | ENSP00000441569.1:p.Ala14= | |
| ENST00000494660.6:c.42A= | ENSP00000437361.1:p.Ala14= | |
| NM_032601.3:c.327A= | NP_115990.3:p.Ala109= | |
| XM_005264613.2:c.216+111A= | XP_005264670.1:n.216+111A= | |
| XR_939729.1:n.396A= | ||
| XR_939729.2:n.396A= | ||
| NM_032601.4:c.327A= MANE Select | NP_115990.3:p.Ala109= |