Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97598871A= , CM000672.2:g.97598871A= | GRCh38 |
| NC_000010.10:g.99358628A= , CM000672.1:g.99358628A= | GRCh37 |
| NC_000010.9:g.99348618A= | NCBI36 |
| NG_027922.1:g.19527A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_138413.4:c.308A= MANE Select | NP_612422.2:p.Asn103= |
| ENST00000370646.9:c.308A= MANE Select | ENSP00000359680.4:p.Asn103= |
| NM_001134670.1:c.212-2986A= | NP_001128142.1:n.212-2986A= |
| NM_001134670.2:c.212-2986A= | NP_001128142.1:n.212-2986A= |
| NM_138413.3:c.308A= | NP_612422.2:p.Asn103= |
| ENST00000370646.8:c.308A= | ENSP00000359680.4:p.Asn103= |
| ENST00000370647.8:c.212-2986A= | ENSP00000359681.4:n.212-2986A= |
| ENST00000370649.3:c.212-2986A= | ENSP00000359683.3:n.212-2986A= |
| ENST00000465608.1:n.689A= |