Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763798G= , CM000674.2:g.57763798G= | GRCh38 |
| NC_000012.11:g.58157581G= , CM000674.1:g.58157581G= | GRCh37 |
| NC_000012.10:g.56443848G= | NCBI36 |
| NG_007076.1:g.8396C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000785.4:c.1226C= MANE Select | NP_000776.1:p.Thr409= |
| ENST00000228606.9:c.1226C= MANE Select | ENSP00000228606.4:p.Thr409= |
| NM_000785.3:c.1226C= | NP_000776.1:p.Thr409= |
| ENST00000228606.8:c.1226C= | ENSP00000228606.4:p.Thr409= |
| ENST00000547344.5:n.1365C= | |
| ENST00000713544.1:c.1307C= | ENSP00000518840.1:p.Thr436= |
| ENST00000713545.1:c.*231C= | ENSP00000518841.1:n.*231C= |