Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52520166C= , CM000674.2:g.52520166C= | GRCh38 |
| NC_000012.11:g.52913950C= , CM000674.1:g.52913950C= | GRCh37 |
| NC_000012.10:g.51200217C= | NCBI36 |
| NG_008297.1:g.5294G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.131G= MANE Select | ENSP00000252242.4:p.Gly44= | |
| ENST00000252242.8:c.131G= | ENSP00000252242.4:p.Gly44= | |
| ENST00000546577.1:c.131G= | ENSP00000449651.1:p.Gly44= | |
| ENST00000549420.1:c.43+88G= | ENSP00000447209.1:n.43+88G= | |
| ENST00000551275.1:c.131G= | ENSP00000448041.1:p.Gly44= | |
| ENST00000552629.5:n.229G= | ||
| NM_000424.3:c.131G= | NP_000415.2:p.Gly44= | |
| NM_000424.4:c.131G= MANE Select | NP_000415.2:p.Gly44= |