Linked Data
MyVariant Identifiers:
chr11:g.299425T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.299425T>A , CM000673.2:g.299425T>A | GRCh38 |
| NC_000011.9:g.299425T>A , CM000673.1:g.299425T>A | GRCh37 |
| NC_000011.8:g.289425T>A | NCBI36 |
| NG_032892.1:g.5102A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382614.2:c.66A>T MANE Select | ENSP00000372059.2:p.Thr22= | |
| NM_001025295.2:c.66A>T | NP_001020466.1:p.Thr22= | |
| NM_001025295.3:c.66A>T MANE Select | NP_001020466.1:p.Thr22= |