Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68444582C>A , CM000663.2:g.68444582C>A | GRCh38 |
| NC_000001.10:g.68910265C>A , CM000663.1:g.68910265C>A | GRCh37 |
| NC_000001.9:g.68682853C>A | NCBI36 |
| NG_008472.1:g.10378G>T | |
| NG_008472.2:g.10378G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000329.3:c.444G>T MANE Select | NP_000320.1:p.Glu148Asp |
| ENST00000262340.6:c.444G>T MANE Select | ENSP00000262340.5:p.Glu148Asp |
| NM_000329.2:c.444G>T | NP_000320.1:p.Glu148Asp |
| ENST00000262340.5:c.444G>T | ENSP00000262340.5:p.Glu148Asp |
| XM_017002027.1:c.168G>T | XP_016857516.1:p.Glu56Asp |