Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.12885540A= , CM000685.2:g.12885540A= | GRCh38 |
| NC_000023.10:g.12903659A= , CM000685.1:g.12903659A= | GRCh37 |
| NC_000023.9:g.12813580A= | NCBI36 |
| NG_012569.1:g.23458A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016562.4:c.32A= MANE Select | NP_057646.1:p.Gln11= |
| ENST00000380659.4:c.32A= MANE Select | ENSP00000370034.3:p.Gln11= |
| NM_016562.3:c.32A= | NP_057646.1:p.Gln11= |
| ENST00000380659.3:c.32A= | ENSP00000370034.3:p.Gln11= |