Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.162254849T= , CM000663.2:g.162254849T= | GRCh38 |
| NC_000001.10:g.162224639T= , CM000663.1:g.162224639T= | GRCh37 |
| NC_000001.9:g.160491263T= | NCBI36 |
| NG_015979.1:g.190059T= | |
| NG_015979.2:g.190059T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361897.10:c.178-32495T= MANE Select | ENSP00000355133.5:n.178-32495T= | |
| ENST00000361897.9:c.178-32495T= | ENSP00000355133.5:n.178-32495T= | |
| ENST00000430120.3:c.178-32495T= | ENSP00000396713.3:n.178-32495T= | |
| ENST00000530878.5:c.178-32495T= | ENSP00000431586.1:n.178-32495T= | |
| NM_001164757.1:c.178-32495T= | NP_001158229.1:n.178-32495T= | |
| NM_014697.2:c.178-32495T= | NP_055512.1:n.178-32495T= | |
| NM_014697.3:c.178-32495T= MANE Select | NP_055512.1:n.178-32495T= | |
| NM_001164757.2:c.178-32495T= | NP_001158229.1:n.178-32495T= |