Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128556302T= , CM000673.2:g.128556302T= | GRCh38 |
| NC_000011.9:g.128426197T= , CM000673.1:g.128426197T= | GRCh37 |
| NC_000011.8:g.127931407T= | NCBI36 |
| NG_029555.1:g.36257A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001143820.2:c.203A= MANE Select | NP_001137292.1:p.His68= |
| ENST00000392668.8:c.203A= MANE Select | ENSP00000376436.3:p.His68= |
| NM_001143820.1:c.203A= | NP_001137292.1:p.His68= |
| ENST00000525404.5:n.272A= | |
| XM_011542649.1:c.203A= | XP_011540951.1:p.His68= |
| XM_011542651.1:c.203A= | XP_011540953.1:p.His68= |
| XM_017017314.1:c.203A= | XP_016872803.1:p.His68= |
| XM_017017315.2:c.98A= | XP_016872804.1:p.His33= |
| XM_017017317.1:c.203A= | XP_016872806.1:p.His68= |