Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30724492A>G , CM000678.2:g.30724492A>G | GRCh38 |
| NC_000016.9:g.30735813A>G , CM000678.1:g.30735813A>G | GRCh37 |
| NC_000016.8:g.30643314A>G | NCBI36 |
| NG_032135.1:g.30352A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006662.3:c.5068A>G MANE Select | NP_006653.2:p.Thr1690Ala |
| ENST00000262518.9:c.5068A>G MANE Select | ENSP00000262518.4:p.Thr1690Ala |
| NM_006662.2:c.5068A>G | NP_006653.2:p.Thr1690Ala |
| ENST00000262518.8:c.5068A>G | ENSP00000262518.4:p.Thr1690Ala |
| ENST00000380361.7:c.4537A>G | ENSP00000369719.3:p.Thr1513Ala |
| ENST00000395059.6:c.4291A>G | ENSP00000378499.3:p.Thr1431Ala |
| ENST00000411466.7:c.5068A>G | ENSP00000405186.3:p.Thr1690Ala |
| ENST00000483083.3:c.4167A>G | |
| ENST00000706321.1:c.5068A>G | ENSP00000516346.1:p.Thr1690Ala |