Linked Data
MyVariant Identifiers:
chr10:g.112337187T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110577429T>G , CM000672.2:g.110577429T>G | GRCh38 |
| NC_000010.10:g.112337187T>G , CM000672.1:g.112337187T>G | GRCh37 |
| NC_000010.9:g.112327177T>G | NCBI36 |
| NG_012217.1:g.14739T>G , LRG_774:g.14739T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.340T>G | ||
| ENST00000687823.1:n.121T>G | ||
| ENST00000689932.1:n.2270T>G | ||
| ENST00000691297.1:n.340T>G | ||
| ENST00000691527.1:n.297T>G | ||
| ENST00000692792.1:n.326T>G | ||
| ENST00000361804.5:c.207T>G MANE Select | ENSP00000354720.5:p.Thr69= | |
| ENST00000361804.4:c.207T>G | ENSP00000354720.4:p.Thr69= | |
| ENST00000462899.1:n.353T>G | ||
| NM_005445.3:c.207T>G , LRG_774t1:c.207T>G | NP_005436.1:p.Thr69= | |
| NM_005445.4:c.207T>G MANE Select | NP_005436.1:p.Thr69= |