Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.6770235T= , CM000682.2:g.6770235T= | GRCh38 |
| NC_000020.10:g.6750882T= , CM000682.1:g.6750882T= | GRCh37 |
| NC_000020.9:g.6698882T= | NCBI36 |
| NG_023233.1:g.7138T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001200.4:c.109T= MANE Select | NP_001191.1:p.Ser37= |
| ENST00000378827.5:c.109T= MANE Select | ENSP00000368104.3:p.Ser37= |
| NM_001200.2:c.109T= | NP_001191.1:p.Ser37= |
| NM_001200.3:c.109T= | NP_001191.1:p.Ser37= |
| ENST00000378827.4:c.109T= | ENSP00000368104.3:p.Ser37= |
| XM_011529323.1:c.-123+1360T= | XP_011527625.1:n.-123+1360T= |