Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185145023G= , CM000666.2:g.185145023G= | GRCh38 |
| NC_000004.11:g.186066177G= , CM000666.1:g.186066177G= | GRCh37 |
| NC_000004.10:g.186303171G= | NCBI36 |
| NG_013001.1:g.6761G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001151.4:c.371G= MANE Select | NP_001142.2:p.Gly124= |
| ENST00000281456.11:c.371G= MANE Select | ENSP00000281456.5:p.Gly124= |
| NM_001151.3:c.371G= | NP_001142.2:p.Gly124= |
| ENST00000281456.10:c.371G= | ENSP00000281456.5:p.Gly124= |
| ENST00000491736.1:c.371G= | ENSP00000476711.1:p.Gly124= |