Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65868576C= , CM000673.2:g.65868576C= | GRCh38 |
| NC_000011.9:g.65636047C= , CM000673.1:g.65636047C= | GRCh37 |
| NC_000011.8:g.65392623C= | NCBI36 |
| NG_012304.2:g.9359G= | |
| NG_053116.1:g.13515C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307998.11:c.781G= MANE Select | ENSP00000309953.6:p.Glu261= | |
| ENST00000307998.10:c.781G= | ENSP00000309953.6:p.Glu261= | |
| ENST00000526628.5:n.1347G= | ||
| ENST00000527969.1:n.1466G= | ||
| ENST00000528176.5:c.781G= | ENSP00000434151.1:p.Glu261= | |
| ENST00000531005.5:n.1775G= | ||
| ENST00000531972.5:c.781G= | ENSP00000435295.1:p.Glu261= | |
| ENST00000532084.5:n.207G= | ||
| NM_016938.4:c.781G= | NP_058634.4:p.Glu261= | |
| NR_037718.1:n.1040G= | ||
| NM_016938.5:c.781G= MANE Select | NP_058634.4:p.Glu261= | |
| NR_037718.2:n.906G= |