Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44376323T= , CM000679.2:g.44376323T= | GRCh38 |
| NC_000017.10:g.42453691T= , CM000679.1:g.42453691T= | GRCh37 |
| NC_000017.9:g.39809217T= | NCBI36 |
| NG_008331.1:g.18183A= , LRG_479:g.18183A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000419.5:c.2333A= MANE Select | NP_000410.2:p.Gln778= |
| ENST00000262407.6:c.2333A= MANE Select | ENSP00000262407.5:p.Gln778= |
| NM_000419.3:c.2333A= , LRG_479t1:c.2333A= | NP_000410.2:p.Gln778= |
| NM_000419.4:c.2333A= | NP_000410.2:p.Gln778= |
| ENST00000262407.5:c.2333A= | ENSP00000262407.5:p.Gln778= |
| ENST00000592462.5:n.1128A= | |
| ENST00000648408.1:c.1764A= | |
| XM_011524749.1:c.2333A= | XP_011523051.1:p.Gln778= |
| XM_011524750.1:c.2333A= | XP_011523052.1:p.Gln778= |