Linked Data
MyVariant Identifiers:
chr15:g.40763472G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40471273G>T , CM000677.2:g.40471273G>T | GRCh38 |
| NC_000015.9:g.40763472G>T , CM000677.1:g.40763472G>T | GRCh37 |
| NC_000015.8:g.38550764G>T | NCBI36 |
| NG_017074.1:g.5313G>T , LRG_600:g.5313G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306243.7:c.60G>T MANE Select | ENSP00000307297.6:p.Arg20= | |
| ENST00000306243.6:c.60G>T | ENSP00000307297.5:p.Arg20= | |
| ENST00000559991.1:c.60G>T | ENSP00000453882.1:p.Arg20= | |
| NM_130468.3:c.60G>T , LRG_600t1:c.60G>T | NP_569735.1:p.Arg20= | |
| NM_130468.4:c.60G>T MANE Select | NP_569735.1:p.Arg20= |