Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.8797627T>C , CM000678.2:g.8797627T>C | GRCh38 |
| NC_000016.9:g.8891484T>C , CM000678.1:g.8891484T>C | GRCh37 |
| NC_000016.8:g.8798985T>C | NCBI36 |
| NG_009209.1:g.4815T>C | |
| NG_033146.1:g.5022A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333050.7:c.-13A>G (TMEM186) MANE Select | ENSP00000331640.6:n.-13A>G | |
| ENST00000333050.6:c.-13A>G (TMEM186) | ENSP00000331640.6:n.-13A>G | |
| ENST00000564869.1:n.16A>G (TMEM186) | ||
| ENST00000566983.5:c.-15-4172T>C (PMM2) | ENSP00000457956.1:n.-15-4172T>C | |
| NM_015421.3:c.-13A>G (TMEM186) | NP_056236.2:n.-13A>G | |
| NM_015421.4:c.-13A>G (TMEM186) MANE Select | NP_056236.2:n.-13A>G |