Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.59443627T= , CM000673.2:g.59443627T= | GRCh38 |
| NC_000011.9:g.59211100T= , CM000673.1:g.59211100T= | GRCh37 |
| NC_000011.8:g.58967676T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641045.1:c.459T= MANE Select | ENSP00000493195.1:p.Val153= | |
| ENST00000302030.2:c.459T= | ENSP00000303096.2:p.Val153= | |
| NM_001004728.1:c.459T= | NP_001004728.1:p.Val153= | |
| XM_011544810.1:c.459T= | XP_011543112.1:p.Val153= | |
| NM_001004728.2:c.459T= MANE Select | NP_001004728.1:p.Val153= |