Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48610772G= , CM000677.2:g.48610772G= | GRCh38 |
| NC_000015.9:g.48902969G= , CM000677.1:g.48902969G= | GRCh37 |
| NC_000015.8:g.46690261G= | NCBI36 |
| NG_008805.2:g.40017C= , LRG_778:g.40017C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.302C= | ENSP00000453958.2:p.Thr101= | |
| ENST00000674301.2:c.302C= | ENSP00000501333.2:p.Thr101= | |
| ENST00000316623.10:c.302C= MANE Select | ENSP00000325527.5:p.Thr101= | |
| ENST00000316623.9:c.302C= | ENSP00000325527.5:p.Thr101= | |
| ENST00000537463.6:c.302C= | ENSP00000440294.2:p.Thr101= | |
| NM_000138.4:c.302C= , LRG_778t1:c.302C= | NP_000129.3:p.Thr101= | |
| NM_000138.5:c.302C= MANE Select | NP_000129.3:p.Thr101= |