Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.50184666G>A , CM000679.2:g.50184666G>A | GRCh38 |
| NC_000017.10:g.48262027G>A , CM000679.1:g.48262027G>A | GRCh37 |
| NC_000017.9:g.45617026G>A | NCBI36 |
| NG_007400.1:g.21974C>T , LRG_1:g.21974C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000088.4:c.*836C>T MANE Select | NP_000079.2:n.*836C>T |
| ENST00000225964.10:c.*836C>T MANE Select | ENSP00000225964.6:n.*836C>T |
| NM_000088.3:c.*836C>T , LRG_1t1:c.*836C>T | NP_000079.2:n.*836C>T |
| ENST00000225964.9:c.*836C>T | ENSP00000225964.5:n.*836C>T |
| XM_005257058.3:c.*836C>T | XP_005257115.2:n.*836C>T |
| XM_005257058.4:c.*836C>T | XP_005257115.2:n.*836C>T |
| XM_005257059.3:c.*836C>T | XP_005257116.2:n.*836C>T |
| XM_005257059.4:c.*836C>T | XP_005257116.2:n.*836C>T |
| XM_011524341.1:c.*836C>T | XP_011522643.1:n.*836C>T |