Linked Data
MyVariant Identifiers:
chr7:g.146829534T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132442T>G , CM000669.2:g.147132442T>G | GRCh38 |
| NC_000007.13:g.146829534T>G , CM000669.1:g.146829534T>G | GRCh37 |
| NC_000007.12:g.146460467T>G | NCBI36 |
| NG_007092.2:g.1021082T>G | |
| NG_007092.3:g.1021442T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1281T>G MANE Select | ENSP00000354778.3:p.Thr427= | |
| ENST00000636561.1:n.1184T>G | ||
| ENST00000636870.1:n.1143T>G | ||
| ENST00000637150.1:n.1210T>G | ||
| ENST00000637694.1:n.1184T>G | ||
| ENST00000637825.1:n.764T>G | ||
| ENST00000638117.1:n.1184T>G | ||
| ENST00000361727.7:c.1281T>G | ENSP00000354778.3:p.Thr427= | |
| NM_014141.5:c.1281T>G | NP_054860.1:p.Thr427= | |
| XM_017011950.2:c.1281T>G | XP_016867439.1:p.Thr427= | |
| NM_014141.6:c.1281T>G MANE Select | NP_054860.1:p.Thr427= |