Linked Data
MyVariant Identifiers:
chr15:g.48766828A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48474631A>T , CM000677.2:g.48474631A>T | GRCh38 |
| NC_000015.9:g.48766828A>T , CM000677.1:g.48766828A>T | GRCh37 |
| NC_000015.8:g.46554120A>T | NCBI36 |
| NG_008805.2:g.176158T>A , LRG_778:g.176158T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.3984T>A | ENSP00000453958.2:p.Ile1328= | |
| ENST00000674301.2:c.3984T>A | ENSP00000501333.2:p.Ile1328= | |
| ENST00000684448.1:n.2658T>A | ||
| ENST00000316623.10:c.3984T>A MANE Select | ENSP00000325527.5:p.Ile1328= | |
| ENST00000316623.9:c.3984T>A | ENSP00000325527.5:p.Ile1328= | |
| ENST00000537463.6:c.656T>A | ENSP00000440294.2:p.Leu219Ter | |
| NM_000138.4:c.3984T>A , LRG_778t1:c.3984T>A | NP_000129.3:p.Ile1328= | |
| NM_000138.5:c.3984T>A MANE Select | NP_000129.3:p.Ile1328= |