Linked Data
dbSNP Id:
rs2135899823
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70206164T>A , CM000673.2:g.70206164T>A | GRCh38 |
| NC_000011.9:g.70052270T>A , CM000673.1:g.70052270T>A | GRCh37 |
| NC_000011.8:g.69729918T>A | NCBI36 |
| NG_027966.1:g.8002T>A , LRG_228:g.8002T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301838.5:c.318T>A MANE Select | ENSP00000301838.5:p.Asp106Glu | |
| ENST00000301838.4:c.318T>A | ENSP00000301838.4:p.Asp106Glu | |
| NM_003824.3:c.318T>A , LRG_228t1:c.318T>A | NP_003815.1:p.Asp106Glu | |
| NM_003824.4:c.318T>A MANE Select | NP_003815.1:p.Asp106Glu |