Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110919113T>G , CM000674.2:g.110919113T>G | GRCh38 |
| NC_000012.11:g.111356917T>G , CM000674.1:g.111356917T>G | GRCh37 |
| NC_000012.10:g.109841300T>G | NCBI36 |
| NG_007554.1:g.6465A>C , LRG_393:g.6465A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000432.4:c.84A>C MANE Select | NP_000423.2:p.Glu28Asp |
| ENST00000228841.15:c.84A>C MANE Select | ENSP00000228841.8:p.Glu28Asp |
| NM_000432.3:c.84A>C , LRG_393t1:c.84A>C | NP_000423.2:p.Glu28Asp |
| ENST00000228841.12:c.84A>C | ENSP00000228841.7:p.Glu28Asp |
| ENST00000546404.1:n.277A>C | |
| ENST00000548438.1:c.84A>C | ENSP00000447154.1:p.Glu28Asp |
| ENST00000663220.1:c.27A>C | ENSP00000499568.1:p.Glu9Asp |