Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50118823C>T , CM000676.2:g.50118823C>T | GRCh38 |
| NC_000014.8:g.50585541C>T , CM000676.1:g.50585541C>T | GRCh37 |
| NC_000014.7:g.49655291C>T | NCBI36 |
| NG_051073.1:g.117871G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006939.4:c.3520G>A MANE Select | NP_008870.2:p.Ala1174Thr |
| ENST00000216373.10:c.3520G>A MANE Select | ENSP00000216373.5:p.Ala1174Thr |
| NM_006939.2:c.3520G>A | NP_008870.2:p.Ala1174Thr |
| NM_006939.3:c.3520G>A | NP_008870.2:p.Ala1174Thr |
| ENST00000216373.9:c.3520G>A | ENSP00000216373.5:p.Ala1174Thr |
| ENST00000543680.5:c.3421G>A | ENSP00000445328.1:p.Ala1141Thr |
| XM_005268021.1:c.3340G>A | XP_005268078.1:p.Ala1114Thr |
| XM_011537103.1:c.3481G>A | XP_011535405.1:p.Ala1161Thr |