Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153261034A= , CM000663.2:g.153261034A= | GRCh38 |
| NC_000001.10:g.153233510A= , CM000663.1:g.153233510A= | GRCh37 |
| NC_000001.9:g.151500134A= | NCBI36 |
| NG_011818.1:g.6332A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000427.3:c.85A= MANE Select | NP_000418.2:p.Ser29= |
| ENST00000368742.4:c.85A= MANE Select | ENSP00000357731.3:p.Ser29= |
| NM_000427.2:c.85A= | NP_000418.2:p.Ser29= |
| ENST00000368742.3:c.85A= | ENSP00000357731.3:p.Ser29= |
| XM_011509541.1:c.85A= | XP_011507843.1:p.Ser29= |
| XM_024447049.1:c.85A= | XP_024302817.1:p.Ser29= |