Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.918462G>T , CM000681.2:g.918462G>T | GRCh38 |
| NC_000019.9:g.918462G>T , CM000681.1:g.918462G>T | GRCh37 |
| NC_000019.8:g.869462G>T | NCBI36 |
| NG_008277.1:g.6121G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234371.10:c.245-82G>T MANE Select | ENSP00000234371.3:n.245-82G>T | |
| ENST00000234371.9:c.245-82G>T | ENSP00000234371.3:n.245-82G>T | |
| ENST00000592648.1:c.244+716G>T | ENSP00000467666.1:n.244+716G>T | |
| ENST00000606939.2:c.245-82G>T | ENSP00000475639.1:n.245-82G>T | |
| NM_032551.4:c.245-82G>T | NP_115940.2:n.245-82G>T | |
| XM_017027382.1:c.245-82G>T | XP_016882871.1:n.245-82G>T | |
| NM_032551.5:c.245-82G>T MANE Select | NP_115940.2:n.245-82G>T |