Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154969444T= , CM000685.2:g.154969444T= | GRCh38 |
| NC_000023.10:g.154197719T= , CM000685.1:g.154197719T= | GRCh37 |
| NC_000023.9:g.153850913T= | NCBI36 |
| NG_011403.1:g.58280A= | |
| NG_011403.2:g.58280A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.896A= MANE Select | NP_000123.1:p.Asn299= |
| ENST00000360256.9:c.896A= MANE Select | ENSP00000353393.4:p.Asn299= |
| NM_000132.3:c.896A= | NP_000123.1:p.Asn299= |
| ENST00000360256.8:c.896A= | ENSP00000353393.4:p.Asn299= |
| ENST00000647125.1:c.*772A= | ENSP00000496062.1:n.*772A= |
| XM_011531126.1:c.791A= | XP_011529428.1:p.Asn264= |