Linked Data
MyVariant Identifiers:
chr9:g.12695546A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12695546A>G , CM000671.2:g.12695546A>G | GRCh38 |
| NC_000009.11:g.12695546A>G , CM000671.1:g.12695546A>G | GRCh37 |
| NC_000009.10:g.12685546A>G | NCBI36 |
| NG_011705.1:g.7161A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.417A>G MANE Select | ENSP00000373570.4:p.Glu139= | |
| ENST00000388918.9:c.417A>G | ENSP00000373570.4:p.Glu139= | |
| NM_000550.2:c.417A>G | NP_000541.1:p.Glu139= | |
| XR_001746372.2:n.606A>G | ||
| NM_000550.3:c.417A>G MANE Select | NP_000541.1:p.Glu139= |