Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15889228A>C , CM000681.2:g.15889228A>C | GRCh38 |
| NC_000019.9:g.16000038A>C , CM000681.1:g.16000038A>C | GRCh37 |
| NC_000019.8:g.15861038A>C | NCBI36 |
| NG_007971.2:g.13847T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.918+195T>G MANE Select | ENSP00000221700.3:n.918+195T>G | |
| ENST00000011989.11:c.918+195T>G | ENSP00000011989.8:n.918+195T>G | |
| ENST00000221700.10:c.918+195T>G | ENSP00000221700.3:n.918+195T>G | |
| ENST00000392846.7:n.861+195T>G | ||
| ENST00000587671.2:c.*503+195T>G | ENSP00000467443.2:n.*503+195T>G | |
| NM_001082.4:c.918+195T>G | NP_001073.3:n.918+195T>G | |
| NM_001082.5:c.918+195T>G MANE Select | NP_001073.3:n.918+195T>G |