Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.129812725T>C , CM000685.2:g.129812725T>C | GRCh38 |
| NC_000023.10:g.128946701T>C , CM000685.1:g.128946701T>C | GRCh37 |
| NC_000023.9:g.128774382T>C | NCBI36 |
| NG_021387.1:g.36210A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016032.4:c.770A>G MANE Select | NP_057116.2:p.Asn257Ser |
| ENST00000357166.11:c.770A>G MANE Select | ENSP00000349689.6:p.Asn257Ser |
| NM_001008222.2:c.770A>G | NP_001008223.1:p.Asn257Ser |
| NM_001008222.3:c.770A>G | NP_001008223.1:p.Asn257Ser |
| NM_016032.3:c.770A>G | NP_057116.2:p.Asn257Ser |
| ENST00000357166.10:c.770A>G | ENSP00000349689.6:p.Asn257Ser |
| ENST00000371064.7:c.770A>G | ENSP00000360103.3:p.Asn257Ser |
| ENST00000433917.5:c.511A>G | |
| XR_001755694.2:n.1274A>G |