Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2718535T>G , CM000671.2:g.2718535T>G | GRCh38 |
| NC_000009.11:g.2718535T>G , CM000671.1:g.2718535T>G | GRCh37 |
| NC_000009.10:g.2708535T>G | NCBI36 |
| NG_012181.1:g.6010T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_133497.4:c.796T>G MANE Select | NP_598004.1:p.Ser266Ala |
| ENST00000382082.4:c.796T>G MANE Select | ENSP00000371514.3:p.Ser266Ala |
| NM_133497.3:c.796T>G | NP_598004.1:p.Ser266Ala |
| ENST00000382082.3:c.796T>G | ENSP00000371514.3:p.Ser266Ala |
| XR_929202.1:n.1297T>G | |
| XR_929203.1:n.1297T>G |