Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.39447012G>C , CM000666.2:g.39447012G>C | GRCh38 |
| NC_000004.11:g.39448632G>C , CM000666.1:g.39448632G>C | GRCh37 |
| NC_000004.10:g.39125027G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000257408.5:c.2286G>C MANE Select | ENSP00000257408.4:p.Glu762Asp | |
| ENST00000257408.4:c.2286G>C | ENSP00000257408.4:p.Glu762Asp | |
| NM_175737.3:c.2286G>C | NP_783864.1:p.Glu762Asp | |
| XM_005262644.1:c.2259G>C | XP_005262701.1:p.Glu753Asp | |
| NM_175737.4:c.2286G>C MANE Select | NP_783864.1:p.Glu762Asp |