Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612294A= , CM000679.2:g.41612294A= | GRCh38 |
| NC_000017.10:g.39768546A= , CM000679.1:g.39768546A= | GRCh37 |
| NC_000017.9:g.37022072A= | NCBI36 |
| NG_008301.1:g.5534T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005557.4:c.395T= MANE Select | NP_005548.2:p.Leu132= |
| ENST00000301653.9:c.395T= MANE Select | ENSP00000301653.3:p.Leu132= |
| NM_005557.3:c.395T= | NP_005548.2:p.Leu132= |
| ENST00000301653.8:c.395T= | ENSP00000301653.3:p.Leu132= |
| ENST00000588319.1:n.472T= | |
| ENST00000593067.1:c.-312-8T= | ENSP00000467124.1:n.-312-8T= |