Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.62447486T= , CM000663.2:g.62447486T= | GRCh38 |
| NC_000001.10:g.62913157T= , CM000663.1:g.62913157T= | GRCh37 |
| NC_000001.9:g.62685745T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000339950.5:c.1395T= MANE Select | ENSP00000343526.4:p.Leu465= | |
| ENST00000339950.4:c.1395T= | ENSP00000343526.4:p.Leu465= | |
| ENST00000371146.5:c.1395T= | ENSP00000360188.1:p.Leu465= | |
| NM_001017415.1:c.1395T= | NP_001017415.1:p.Leu465= | |
| NM_001017416.1:c.1395T= | NP_001017416.1:p.Leu465= | |
| NM_003368.4:c.1395T= | NP_003359.3:p.Leu465= | |
| NM_003368.5:c.1395T= MANE Select | NP_003359.3:p.Leu465= | |
| NM_001017415.2:c.1395T= | NP_001017415.1:p.Leu465= | |
| NM_001017416.2:c.1395T= | NP_001017416.1:p.Leu465= |