Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924315G= , CM000675.2:g.27924315G= | GRCh38 |
| NC_000013.10:g.28498452G= , CM000675.1:g.28498452G= | GRCh37 |
| NC_000013.9:g.27396452G= | NCBI36 |
| NG_008183.1:g.9285G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.466G= MANE Select | ENSP00000370421.4:p.Ala156= | |
| ENST00000381033.4:c.466G= | ENSP00000370421.4:p.Ala156= | |
| NM_000209.3:c.466G= | NP_000200.1:p.Ala156= | |
| XR_941579.1:n.2192G= | ||
| XR_941580.1:n.1108G= | ||
| XR_941580.2:n.1120G= | ||
| NM_000209.4:c.466G= MANE Select | NP_000200.1:p.Ala156= |