Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272840C= , CM000676.2:g.91272840C= | GRCh38 |
| NC_000014.8:g.91739184C= , CM000676.1:g.91739184C= | GRCh37 |
| NC_000014.7:g.90808937C= | NCBI36 |
| NG_033118.1:g.150005G= | |
| NG_033118.2:g.150005G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5872G= MANE Select | ENSP00000374507.6:p.Ala1958= | |
| ENST00000331194.8:c.1306G= | ENSP00000330332.8:p.Ala436= | |
| ENST00000389857.10:c.5872G= | ENSP00000374507.6:p.Ala1958= | |
| ENST00000556726.5:c.2100G= | ||
| NM_001080414.3:c.5872G= | NP_001073883.2:p.Ala1958= | |
| XM_011536796.1:c.5764G= | XP_011535098.1:p.Ala1922= | |
| XM_011536796.2:c.5764G= | XP_011535098.1:p.Ala1922= | |
| XM_017021336.1:c.2953G= | XP_016876825.1:p.Ala985= | |
| NM_001080414.4:c.5872G= MANE Select | NP_001073883.2:p.Ala1958= |