Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80273865C= , CM000672.2:g.80273865C= | GRCh38 |
| NC_000010.10:g.82033621C= , CM000672.1:g.82033621C= | GRCh37 |
| NC_000010.9:g.82023601C= | NCBI36 |
| NG_008083.1:g.20814G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1104G= MANE Select | ENSP00000361287.3:p.Lys368= | |
| ENST00000372213.7:c.1104G= | ENSP00000361287.3:p.Lys368= | |
| ENST00000480845.1:n.336G= | ||
| ENST00000485270.5:n.616G= | ||
| NM_000429.2:c.1104G= | NP_000420.1:p.Lys368= | |
| XM_005269842.3:c.1104G= | XP_005269899.1:p.Lys368= | |
| XM_005269843.3:c.981G= | XP_005269900.1:p.Lys327= | |
| NM_000429.3:c.1104G= MANE Select | NP_000420.1:p.Lys368= |