Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.38396892G= , CM000671.2:g.38396892G= | GRCh38 |
| NC_000009.11:g.38396889G= , CM000671.1:g.38396889G= | GRCh37 |
| NC_000009.10:g.38386889G= | NCBI36 |
| NG_012253.1:g.9188G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377698.4:c.1144G= MANE Select | ENSP00000366927.3:p.Ala382= | |
| ENST00000377698.3:c.1144G= | ENSP00000366927.3:p.Ala382= | |
| NM_000692.4:c.1144G= | NP_000683.3:p.Ala382= | |
| XM_011517802.1:c.1144G= | XP_011516104.1:p.Ala382= | |
| XM_011517802.2:c.1144G= | XP_011516104.1:p.Ala382= | |
| NM_000692.5:c.1144G= MANE Select | NP_000683.3:p.Ala382= |