Linked Data
MyVariant Identifiers:
chr11:g.5246882G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225652G>A , CM000673.2:g.5225652G>A | GRCh38 |
| NC_000011.9:g.5246882G>A , CM000673.1:g.5246882G>A | GRCh37 |
| NC_000011.8:g.5203458G>A | NCBI36 |
| NG_000007.3:g.71964C>T | |
| NG_059281.1:g.6420C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.390C>T | ENSP00000494175.1:p.Ala130= | |
| ENST00000335295.4:c.390C>T MANE Select | ENSP00000333994.3:p.Ala130= | |
| ENST00000633227.1:c.*206C>T | ENSP00000488004.1:n.*206C>T | |
| NM_000518.4:c.390C>T | NP_000509.1:p.Ala130= | |
| NM_000518.5:c.390C>T MANE Select | NP_000509.1:p.Ala130= |