Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169555336C= , CM000663.2:g.169555336C= | GRCh38 |
| NC_000001.10:g.169524574C= , CM000663.1:g.169524574C= | GRCh37 |
| NC_000001.9:g.167791198C= | NCBI36 |
| NG_011806.1:g.36196G= , LRG_553:g.36196G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.964G= MANE Select | ENSP00000356771.3:p.Ala322= | |
| ENST00000367796.3:c.964G= | ENSP00000356770.3:p.Ala322= | |
| ENST00000367797.7:c.964G= | ENSP00000356771.3:p.Ala322= | |
| NM_000130.4:c.964G= , LRG_553t1:c.964G= | NP_000121.2:p.Ala322= | |
| XM_017000660.2:c.553G= | XP_016856149.1:p.Ala185= | |
| NM_000130.5:c.964G= MANE Select | NP_000121.2:p.Ala322= |