Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94030506T>G , CM000663.2:g.94030506T>G | GRCh38 |
| NC_000001.10:g.94496062T>G , CM000663.1:g.94496062T>G | GRCh37 |
| NC_000001.9:g.94268650T>G | NCBI36 |
| NG_009073.1:g.95644A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4274A>C MANE Select | ENSP00000359245.3:p.Glu1425Ala | |
| ENST00000370225.3:c.4274A>C | ENSP00000359245.3:p.Glu1425Ala | |
| ENST00000536513.5:c.650A>C | ENSP00000439707.2:p.Glu217Ala | |
| NM_000350.2:c.4274A>C | NP_000341.2:p.Glu1425Ala | |
| NM_000350.3:c.4274A>C MANE Select | NP_000341.2:p.Glu1425Ala |