Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30308222A= , CM000685.2:g.30308222A= | GRCh38 |
| NC_000023.10:g.30326339A= , CM000685.1:g.30326339A= | GRCh37 |
| NC_000023.9:g.30236260A= | NCBI36 |
| NG_009814.1:g.6157T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000475.5:c.1142T= MANE Select | NP_000466.2:p.Leu381= |
| ENST00000378970.5:c.1142T= MANE Select | ENSP00000368253.4:p.Leu381= |
| NM_000475.4:c.1142T= | NP_000466.2:p.Leu381= |
| ENST00000378963.1:c.257T= | ENSP00000368246.1:p.Leu86= |
| ENST00000378970.4:c.1142T= | ENSP00000368253.4:p.Leu381= |