Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.8797601C= , CM000678.2:g.8797601C= | GRCh38 |
| NC_000016.9:g.8891458C= , CM000678.1:g.8891458C= | GRCh37 |
| NC_000016.8:g.8798959C= | NCBI36 |
| NG_009209.1:g.4789C= | |
| NG_033146.1:g.5048G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333050.7:c.3+11G= (TMEM186) MANE Select | ENSP00000331640.6:n.3+11G= | |
| ENST00000333050.6:c.3+11G= (TMEM186) | ENSP00000331640.6:n.3+11G= | |
| ENST00000564869.1:n.31+11G= (TMEM186) | ||
| ENST00000566983.5:c.-15-4198C= (PMM2) | ENSP00000457956.1:n.-15-4198C= | |
| NM_015421.3:c.3+11G= (TMEM186) | NP_056236.2:n.3+11G= | |
| NM_015421.4:c.3+11G= (TMEM186) MANE Select | NP_056236.2:n.3+11G= |