Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25015640A= , CM000685.2:g.25015640A= | GRCh38 |
| NC_000023.10:g.25033757A= , CM000685.1:g.25033757A= | GRCh37 |
| NC_000023.9:g.24943678A= | NCBI36 |
| NG_008281.1:g.5309T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139058.3:c.98T= MANE Select | NP_620689.1:p.Leu33= |
| ENST00000379044.5:c.98T= MANE Select | ENSP00000368332.4:p.Leu33= |
| NM_139058.2:c.98T= | NP_620689.1:p.Leu33= |
| ENST00000379044.4:c.98T= | ENSP00000368332.4:p.Leu33= |
| ENST00000636609.1:n.41T= | |
| ENST00000637394.1:n.73T= |