Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.5692831G= , CM000664.2:g.5692831G= | GRCh38 |
| NC_000002.11:g.5832963G= , CM000664.1:g.5832963G= | GRCh37 |
| NC_000002.10:g.5750414G= | NCBI36 |
| NG_050751.1:g.5165G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322002.5:c.110G= MANE Select | ENSP00000322568.3:p.Ser37= | |
| ENST00000322002.4:c.110G= | ENSP00000322568.3:p.Ser37= | |
| NM_003108.3:c.110G= | NP_003099.1:p.Ser37= | |
| NM_003108.4:c.110G= MANE Select | NP_003099.1:p.Ser37= |