Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15445679G= , CM000663.2:g.15445679G= | GRCh38 |
| NC_000001.10:g.15772174G= , CM000663.1:g.15772174G= | GRCh37 |
| NC_000001.9:g.15644761G= | NCBI36 |
| NG_009253.1:g.12237G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375949.5:c.722G= MANE Select | ENSP00000365116.4:p.Arg241= | |
| ENST00000375943.6:c.*176G= | ENSP00000365110.2:n.*176G= | |
| ENST00000375949.4:c.722G= | ENSP00000365116.4:p.Arg241= | |
| ENST00000483406.1:n.486G= | ||
| NM_007272.2:c.722G= | NP_009203.2:p.Arg241= | |
| XM_011540550.1:c.576G= | XP_011538852.1:p.Ala192= | |
| NM_007272.3:c.722G= MANE Select | NP_009203.2:p.Arg241= |