Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63957443C= , CM000679.2:g.63957443C= | GRCh38 |
| NC_000017.10:g.62034803C= , CM000679.1:g.62034803C= | GRCh37 |
| NC_000017.9:g.59388535C= | NCBI36 |
| NG_011699.1:g.20476G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000334.4:c.2095G= MANE Select | NP_000325.4:p.Ala699= |
| ENST00000435607.3:c.2095G= MANE Select | ENSP00000396320.1:p.Ala699= |
| ENST00000578147.5:c.2095G= | ENSP00000463963.1:p.Ala699= |
| XM_005257566.3:c.2095G= | XP_005257623.1:p.Ala699= |