Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215675271T= , CM000663.2:g.215675271T= | GRCh38 |
| NC_000001.10:g.215848613T= , CM000663.1:g.215848613T= | GRCh37 |
| NC_000001.9:g.213915236T= | NCBI36 |
| NG_009497.1:g.753126A= | |
| NG_009497.2:g.753178A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.12640A= MANE Select | ENSP00000305941.3:p.Thr4214= | |
| ENST00000674083.1:c.12640A= | ENSP00000501296.1:p.Thr4214= | |
| ENST00000307340.7:c.12640A= | ENSP00000305941.3:p.Thr4214= | |
| NM_206933.2:c.12640A= | NP_996816.2:p.Thr4214= | |
| NM_206933.3:c.12640A= | NP_996816.2:p.Thr4214= | |
| NM_206933.4:c.12640A= MANE Select | NP_996816.3:p.Thr4214= |