Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47406919A= , CM000666.2:g.47406919A= | GRCh38 |
| NC_000004.11:g.47408936A= , CM000666.1:g.47408936A= | GRCh37 |
| NC_000004.10:g.47103693A= | NCBI36 |
| NG_051831.1:g.380642A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295454.8:c.1073A= MANE Select | ENSP00000295454.3:p.Lys358= | |
| ENST00000295454.7:c.1073A= | ENSP00000295454.3:p.Lys358= | |
| NM_000812.3:c.1073A= | NP_000803.2:p.Lys358= | |
| XM_011513678.1:c.1052A= | XP_011511980.1:p.Lys351= | |
| XM_017007985.1:c.422A= | XP_016863474.1:p.Lys141= | |
| XM_024453976.1:c.974A= | XP_024309744.1:p.Lys325= | |
| XM_024453977.1:c.974A= | XP_024309745.1:p.Lys325= | |
| XM_024453978.1:c.974A= | XP_024309746.1:p.Lys325= | |
| NM_000812.4:c.1073A= MANE Select | NP_000803.2:p.Lys358= |