Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4899036C= , CM000679.2:g.4899036C= | GRCh38 |
| NC_000017.10:g.4802331C= , CM000679.1:g.4802331C= | GRCh37 |
| NC_000017.9:g.4743110C= | NCBI36 |
| NG_008029.2:g.9040G= | |
| NG_028005.1:g.70697C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000080.4:c.1291G= MANE Select | NP_000071.1:p.Ala431= |
| ENST00000649488.2:c.1291G= MANE Select | ENSP00000497829.1:p.Ala431= |
| NM_000080.3:c.1291G= | NP_000071.1:p.Ala431= |
| ENST00000293780.4:c.1291G= | ENSP00000293780.4:p.Ala431= |
| ENST00000572438.1:n.977G= | |
| ENST00000649830.1:c.358G= | ENSP00000496907.1:p.Ala120= |
| ENST00000652550.1:n.1021G= | |
| XM_017024115.1:c.1255G= | XP_016879604.1:p.Ala419= |