Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107710201T= , CM000669.2:g.107710201T= | GRCh38 |
| NC_000007.13:g.107350646T= , CM000669.1:g.107350646T= | GRCh37 |
| NC_000007.12:g.107137882T= | NCBI36 |
| NG_008489.1:g.54567T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2235+2T= MANE Select | ENSP00000494017.1:n.2235+2T= | |
| ENST00000644846.1:c.891+2T= | ||
| ENST00000265715.7:c.2235+2T= | ENSP00000265715.3:n.2235+2T= | |
| ENST00000492030.2:n.421+2T= | ||
| NM_000441.1:c.2235+2T= | NP_000432.1:n.2235+2T= | |
| XM_005250425.1:c.2235+2T= | XP_005250482.1:n.2235+2T= | |
| XM_005250425.2:c.2235+2T= | XP_005250482.1:n.2235+2T= | |
| XM_017012318.1:c.2157+2T= | XP_016867807.1:n.2157+2T= | |
| NM_000441.2:c.2235+2T= MANE Select | NP_000432.1:n.2235+2T= |