Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30737276T>A , CM000678.2:g.30737276T>A | GRCh38 |
| NC_000016.9:g.30748597T>A , CM000678.1:g.30748597T>A | GRCh37 |
| NC_000016.8:g.30656098T>A | NCBI36 |
| NG_032135.1:g.43136T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411466.7:c.7236T>A | ENSP00000405186.3:p.Thr2412= | |
| ENST00000704023.1:c.1516T>A | ||
| ENST00000706321.1:c.7236T>A | ENSP00000516346.1:p.Thr2412= | |
| ENST00000262518.9:c.7236T>A MANE Select | ENSP00000262518.4:p.Thr2412= | |
| ENST00000262518.8:c.7236T>A | ENSP00000262518.4:p.Thr2412= | |
| ENST00000380361.7:c.6705T>A | ENSP00000369719.3:p.Thr2235= | |
| ENST00000395059.6:c.6459T>A | ENSP00000378499.3:p.Thr2153= | |
| NM_006662.2:c.7236T>A | NP_006653.2:p.Thr2412= | |
| NM_006662.3:c.7236T>A MANE Select | NP_006653.2:p.Thr2412= |