Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.104801767G= , CM000676.2:g.104801767G= | GRCh38 |
| NC_000014.8:g.105268104G= , CM000676.1:g.105268104G= | GRCh37 |
| NC_000014.7:g.104339149G= | NCBI36 |
| NG_042073.1:g.5587G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001137601.3:c.570G= MANE Select | NP_001131073.1:p.Leu190= |
| ENST00000342537.8:c.570G= MANE Select | ENSP00000409107.2:p.Leu190= |
| NM_001137601.1:c.570G= | NP_001131073.1:p.Leu190= |
| NM_001137601.2:c.570G= | NP_001131073.1:p.Leu190= |
| NM_001370342.1:c.570G= | NP_001357271.1:p.Leu190= |
| ENST00000342537.7:c.570G= | ENSP00000409107.2:p.Leu190= |
| ENST00000555360.1:c.570G= | ENSP00000450673.1:p.Leu190= |
| XM_017020911.1:c.570G= | XP_016876400.1:p.Leu190= |