Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.87811540G= , CM000666.2:g.87811540G= | GRCh38 |
| NC_000004.11:g.88732692G= , CM000666.1:g.88732692G= | GRCh37 |
| NC_000004.10:g.88951716G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004967.4:c.584G= MANE Select | NP_004958.2:p.Gly195= |
| ENST00000226284.7:c.584G= MANE Select | ENSP00000226284.5:p.Gly195= |
| NM_004967.3:c.584G= | NP_004958.2:p.Gly195= |
| ENST00000226284.6:c.584G= | ENSP00000226284.5:p.Gly195= |