Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24178241C= , CM000668.2:g.24178241C= | GRCh38 |
| NC_000006.11:g.24178469C= , CM000668.1:g.24178469C= | GRCh37 |
| NC_000006.10:g.24286448C= | NCBI36 |
| NG_012829.1:g.184812G= | |
| NG_012829.2:g.210052G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.1326+89G= MANE Select | ENSP00000367715.3:n.1326+89G= | |
| ENST00000378450.6:c.585+89G= | ENSP00000367711.3:n.585+89G= | |
| ENST00000378454.7:c.1326+89G= | ENSP00000367715.3:n.1326+89G= | |
| NM_001195610.1:c.1326+89G= | NP_001182539.1:n.1326+89G= | |
| NM_016356.4:c.1326+89G= | NP_057440.2:n.1326+89G= | |
| NM_016356.5:c.1326+89G= MANE Select | NP_057440.2:n.1326+89G= | |
| NM_001195610.2:c.1326+89G= | NP_001182539.1:n.1326+89G= |