Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.75769708A= , CM000669.2:g.75769708A= | GRCh38 |
| NC_000007.13:g.75399026A= , CM000669.1:g.75399026A= | GRCh37 |
| NC_000007.12:g.75236962A= | NCBI36 |
| NG_015989.1:g.25039T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000005180.9:c.270T= MANE Select | ENSP00000005180.4:p.Thr90= | |
| ENST00000005180.8:c.270T= | ENSP00000005180.4:p.Thr90= | |
| ENST00000394905.2:c.270T= | ENSP00000378365.2:p.Thr90= | |
| NM_006072.4:c.270T= | NP_006063.1:p.Thr90= | |
| XM_017011671.1:c.432T= | XP_016867160.1:p.Thr144= | |
| XM_017011672.1:c.270T= | XP_016867161.1:p.Thr90= | |
| NM_001371936.1:c.270T= | NP_001358865.1:p.Thr90= | |
| NM_001371938.1:c.270T= MANE Select | NP_001358867.1:p.Thr90= |