Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31519812A= , CM000680.2:g.31519812A= | GRCh38 |
| NC_000018.9:g.29099775A= , CM000680.1:g.29099775A= | GRCh37 |
| NC_000018.8:g.27353773A= | NCBI36 |
| NG_007072.3:g.26571A= , LRG_397:g.26571A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001943.5:c.91A= MANE Select | NP_001934.2:p.Thr31= |
| ENST00000261590.13:c.91A= MANE Select | ENSP00000261590.8:p.Thr31= |
| NM_001943.3:c.91A= , LRG_397t1:c.91A= | NP_001934.2:p.Thr31= |
| NM_001943.4:c.91A= | NP_001934.2:p.Thr31= |
| ENST00000261590.12:c.91A= | ENSP00000261590.8:p.Thr31= |
| ENST00000585206.1:c.91A= | ENSP00000462503.1:p.Thr31= |
| ENST00000682241.2:c.91A= | ENSP00000507600.2:p.Thr31= |
| ENST00000683654.1:c.91A= | ENSP00000506971.1:p.Thr31= |
| XM_024451095.1:c.-444A= | XP_024306863.1:n.-444A= |