Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418513A>G , CM000663.2:g.94418513A>G | GRCh38 |
| NC_000001.10:g.94884069A>G , CM000663.1:g.94884069A>G | GRCh37 |
| NC_000001.9:g.94656657A>G | NCBI36 |
| NG_008865.1:g.5137A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.35A>G MANE Select | ENSP00000359233.4:p.Asn12Ser | |
| ENST00000647998.2:c.35A>G | ENSP00000497921.2:p.Asn12Ser | |
| ENST00000315713.5:c.35A>G | ENSP00000326880.5:p.Asn12Ser | |
| ENST00000370214.8:c.35A>G | ENSP00000359233.4:p.Asn12Ser | |
| NM_001122674.1:c.35A>G | NP_001116146.1:p.Asn12Ser | |
| NM_002858.3:c.35A>G | NP_002849.1:p.Asn12Ser | |
| XM_006710802.2:c.35A>G | XP_006710865.2:p.Asn12Ser | |
| NM_002858.4:c.35A>G MANE Select | NP_002849.1:p.Asn12Ser | |
| NM_001122674.2:c.35A>G | NP_001116146.1:p.Asn12Ser |