Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48497145C= , CM000677.2:g.48497145C= | GRCh38 |
| NC_000015.9:g.48789342C= , CM000677.1:g.48789342C= | GRCh37 |
| NC_000015.8:g.46576634C= | NCBI36 |
| NG_008805.2:g.153644G= , LRG_778:g.153644G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2293+121G= | ENSP00000453958.2:n.2293+121G= | |
| ENST00000674301.2:c.2293+121G= | ENSP00000501333.2:n.2293+121G= | |
| ENST00000684448.1:n.967+121G= | ||
| ENST00000316623.10:c.2293+121G= MANE Select | ENSP00000325527.5:n.2293+121G= | |
| ENST00000316623.9:c.2293+121G= | ENSP00000325527.5:n.2293+121G= | |
| ENST00000537463.6:c.637-22495G= | ENSP00000440294.2:n.637-22495G= | |
| NM_000138.4:c.2293+121G= , LRG_778t1:c.2293+121G= | NP_000129.3:n.2293+121G= | |
| NM_000138.5:c.2293+121G= MANE Select | NP_000129.3:n.2293+121G= |