Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24178082A= , CM000668.2:g.24178082A= | GRCh38 |
| NC_000006.11:g.24178310A= , CM000668.1:g.24178310A= | GRCh37 |
| NC_000006.10:g.24286289A= | NCBI36 |
| NG_012829.1:g.184971T= | |
| NG_012829.2:g.210211T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378454.8:c.1326+248T= MANE Select | ENSP00000367715.3:n.1326+248T= | |
| ENST00000378450.6:c.585+248T= | ENSP00000367711.3:n.585+248T= | |
| ENST00000378454.7:c.1326+248T= | ENSP00000367715.3:n.1326+248T= | |
| NM_001195610.1:c.1326+248T= | NP_001182539.1:n.1326+248T= | |
| NM_016356.4:c.1326+248T= | NP_057440.2:n.1326+248T= | |
| NM_016356.5:c.1326+248T= MANE Select | NP_057440.2:n.1326+248T= | |
| NM_001195610.2:c.1326+248T= | NP_001182539.1:n.1326+248T= |