Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.35663574G= , CM000673.2:g.35663574G= | GRCh38 |
| NC_000011.9:g.35685122G= , CM000673.1:g.35685122G= | GRCh37 |
| NC_000011.8:g.35641698G= | NCBI36 |
| NG_052784.1:g.5883G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017583.6:c.463G= MANE Select | NP_060053.2:p.Gly155= |
| ENST00000299413.7:c.463G= MANE Select | ENSP00000299413.5:p.Gly155= |
| NM_017583.5:c.463G= | NP_060053.2:p.Gly155= |
| ENST00000299413.6:c.463G= | ENSP00000299413.5:p.Gly155= |
| XM_006718254.1:c.463G= | XP_006718317.1:p.Gly155= |