Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15446006T= , CM000663.2:g.15446006T= | GRCh38 |
| NC_000001.10:g.15772501T= , CM000663.1:g.15772501T= | GRCh37 |
| NC_000001.9:g.15645088T= | NCBI36 |
| NG_009253.1:g.12564T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.792+257T= MANE Select | ENSP00000365116.4:n.792+257T= | |
| ENST00000375943.6:c.*246+257T= | ENSP00000365110.2:n.*246+257T= | |
| ENST00000375949.4:c.792+257T= | ENSP00000365116.4:n.792+257T= | |
| ENST00000483406.1:n.556+257T= | ||
| NM_007272.2:c.792+257T= | NP_009203.2:n.792+257T= | |
| XM_011540550.1:c.646+257T= | XP_011538852.1:n.646+257T= | |
| NM_007272.3:c.792+257T= MANE Select | NP_009203.2:n.792+257T= |