Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432568C= , CM000663.2:g.229432568C= | GRCh38 |
| NC_000001.10:g.229568315C= , CM000663.1:g.229568315C= | GRCh37 |
| NC_000001.9:g.227634938C= | NCBI36 |
| NG_006672.1:g.6529G= , LRG_429:g.6529G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001100.4:c.442G= MANE Select | NP_001091.1:p.Gly148= |
| ENST00000366684.7:c.442G= MANE Select | ENSP00000355645.3:p.Gly148= |
| NM_001100.3:c.442G= , LRG_429t1:c.442G= | NP_001091.1:p.Gly148= |
| ENST00000366683.3:c.442G= | ENSP00000355644.3:p.Gly148= |
| ENST00000366683.4:c.442G= | ENSP00000355644.4:p.Gly148= |
| ENST00000684723.1:c.307G= | ENSP00000508084.1:p.Gly103= |