Linked Data
MyVariant Identifiers:
chr11:g.70052279G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.70206173G>A , CM000673.2:g.70206173G>A | GRCh38 |
| NC_000011.9:g.70052279G>A , CM000673.1:g.70052279G>A | GRCh37 |
| NC_000011.8:g.69729927G>A | NCBI36 |
| NG_027966.1:g.8011G>A , LRG_228:g.8011G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301838.5:c.327G>A MANE Select | ENSP00000301838.5:p.Gly109= | |
| ENST00000301838.4:c.327G>A | ENSP00000301838.4:p.Gly109= | |
| NM_003824.3:c.327G>A , LRG_228t1:c.327G>A | NP_003815.1:p.Gly109= | |
| NM_003824.4:c.327G>A MANE Select | NP_003815.1:p.Gly109= |