Linked Data
MyVariant Identifiers:
chr20:g.3065276G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3084630G>T , CM000682.2:g.3084630G>T | GRCh38 |
| NC_000020.10:g.3065276G>T , CM000682.1:g.3065276G>T | GRCh37 |
| NC_000020.9:g.3013276G>T | NCBI36 |
| NG_008663.1:g.5095C>A , LRG_715:g.5095C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.45C>A MANE Select | ENSP00000369647.3:p.Ala15= | |
| NM_000490.4:c.45C>A , LRG_715t1:c.45C>A | NP_000481.2:p.Ala15= | |
| XM_011529267.1:c.45C>A | XP_011527569.1:p.Ala15= | |
| XM_011529267.2:c.45C>A | XP_011527569.1:p.Ala15= | |
| NM_000490.5:c.45C>A MANE Select | NP_000481.2:p.Ala15= |