Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50185602G= , CM000679.2:g.50185602G= | GRCh38 |
| NC_000017.10:g.48262963G= , CM000679.1:g.48262963G= | GRCh37 |
| NC_000017.9:g.45617962G= | NCBI36 |
| NG_007400.1:g.21038C= , LRG_1:g.21038C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225964.10:c.4295C= MANE Select | ENSP00000225964.6:p.Thr1432= | |
| ENST00000225964.9:c.4295C= | ENSP00000225964.5:p.Thr1432= | |
| NM_000088.3:c.4295C= , LRG_1t1:c.4295C= | NP_000079.2:p.Thr1432= | |
| XM_005257058.3:c.4025C= | XP_005257115.2:p.Thr1342= | |
| XM_005257059.3:c.3377C= | XP_005257116.2:p.Thr1126= | |
| XM_011524341.1:c.4097C= | XP_011522643.1:p.Thr1366= | |
| XM_005257058.4:c.4025C= | XP_005257115.2:p.Thr1342= | |
| XM_005257059.4:c.3377C= | XP_005257116.2:p.Thr1126= | |
| NM_000088.4:c.4295C= MANE Select | NP_000079.2:p.Thr1432= |