Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.39587416A>G , CM000677.2:g.39587416A>G | GRCh38 |
| NC_000015.9:g.39879617A>G , CM000677.1:g.39879617A>G | GRCh37 |
| NC_000015.8:g.37666909A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260356.6:c.1190A>G MANE Select | ENSP00000260356.5:p.Asn397Ser | |
| ENST00000260356.5:c.1190A>G | ENSP00000260356.5:p.Asn397Ser | |
| NM_003246.2:c.1190A>G | NP_003237.2:p.Asn397Ser | |
| NM_003246.3:c.1190A>G | NP_003237.2:p.Asn397Ser | |
| XM_011521970.1:c.1190A>G | XP_011520272.1:p.Asn397Ser | |
| XM_011521971.1:c.1190A>G | XP_011520273.1:p.Asn397Ser | |
| XR_931897.1:n.1365A>G | ||
| XM_011521971.2:c.1190A>G | XP_011520273.1:p.Asn397Ser | |
| NM_003246.4:c.1190A>G MANE Select | NP_003237.2:p.Asn397Ser |