Linked Data
MyVariant Identifiers:
chr15:g.48760625A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48468428A>T , CM000677.2:g.48468428A>T | GRCh38 |
| NC_000015.9:g.48760625A>T , CM000677.1:g.48760625A>T | GRCh37 |
| NC_000015.8:g.46547917A>T | NCBI36 |
| NG_008805.2:g.182361T>A , LRG_778:g.182361T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4566T>A | ENSP00000453958.2:p.Thr1522= | |
| ENST00000674301.2:c.4566T>A | ENSP00000501333.2:p.Thr1522= | |
| ENST00000684448.1:n.3240T>A | ||
| ENST00000316623.10:c.4566T>A MANE Select | ENSP00000325527.5:p.Thr1522= | |
| ENST00000316623.9:c.4566T>A | ENSP00000325527.5:p.Thr1522= | |
| ENST00000537463.6:c.*329T>A | ENSP00000440294.2:n.*329T>A | |
| NM_000138.4:c.4566T>A , LRG_778t1:c.4566T>A | NP_000129.3:p.Thr1522= | |
| NM_000138.5:c.4566T>A MANE Select | NP_000129.3:p.Thr1522= |