Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445535T= , CM000663.2:g.15445535T= | GRCh38 |
| NC_000001.10:g.15772030T= , CM000663.1:g.15772030T= | GRCh37 |
| NC_000001.9:g.15644617T= | NCBI36 |
| NG_009253.1:g.12093T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.640-62T= MANE Select | ENSP00000365116.4:n.640-62T= | |
| ENST00000375943.6:c.*94-62T= | ENSP00000365110.2:n.*94-62T= | |
| ENST00000375949.4:c.640-62T= | ENSP00000365116.4:n.640-62T= | |
| ENST00000483406.1:n.404-62T= | ||
| NM_007272.2:c.640-62T= | NP_009203.2:n.640-62T= | |
| XM_011540550.1:c.494-62T= | XP_011538852.1:n.494-62T= | |
| NM_007272.3:c.640-62T= MANE Select | NP_009203.2:n.640-62T= |