Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86670947T= , CM000670.2:g.86670947T= | GRCh38 |
| NC_000008.10:g.87683175T= , CM000670.1:g.87683175T= | GRCh37 |
| NC_000008.9:g.87752291T= | NCBI36 |
| NG_016980.1:g.77729A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.490A= MANE Select | ENSP00000316605.5:p.Thr164= | |
| ENST00000680314.1:n.251A= | ||
| ENST00000681746.1:c.490A= | ENSP00000505959.1:p.Thr164= | |
| ENST00000320005.5:c.490A= | ENSP00000316605.5:p.Thr164= | |
| NM_019098.4:c.490A= | NP_061971.3:p.Thr164= | |
| XM_011517138.1:c.76A= | XP_011515440.1:p.Thr26= | |
| XM_011517138.2:c.76A= | XP_011515440.1:p.Thr26= | |
| NM_019098.5:c.490A= MANE Select | NP_061971.3:p.Thr164= |