Linked Data
MyVariant Identifiers:
chr11:g.299458C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.299458C>A , CM000673.2:g.299458C>A | GRCh38 |
| NC_000011.9:g.299458C>A , CM000673.1:g.299458C>A | GRCh37 |
| NC_000011.8:g.289458C>A | NCBI36 |
| NG_032892.1:g.5069G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382614.2:c.33G>T MANE Select | ENSP00000372059.2:p.Arg11= | |
| NM_001025295.2:c.33G>T | NP_001020466.1:p.Arg11= | |
| NM_001025295.3:c.33G>T MANE Select | NP_001020466.1:p.Arg11= |