Linked Data
MyVariant Identifiers:
chr15:g.48782172T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48489975T>A , CM000677.2:g.48489975T>A | GRCh38 |
| NC_000015.9:g.48782172T>A , CM000677.1:g.48782172T>A | GRCh37 |
| NC_000015.8:g.46569464T>A | NCBI36 |
| NG_008805.2:g.160814A>T , LRG_778:g.160814A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.2958A>T | ENSP00000453958.2:p.Ala986= | |
| ENST00000674301.2:c.2958A>T | ENSP00000501333.2:p.Ala986= | |
| ENST00000684448.1:n.1632A>T | ||
| ENST00000316623.10:c.2958A>T MANE Select | ENSP00000325527.5:p.Ala986= | |
| ENST00000316623.9:c.2958A>T | ENSP00000325527.5:p.Ala986= | |
| ENST00000537463.6:c.637-15325A>T | ENSP00000440294.2:n.637-15325A>T | |
| NM_000138.4:c.2958A>T , LRG_778t1:c.2958A>T | NP_000129.3:p.Ala986= | |
| NM_000138.5:c.2958A>T MANE Select | NP_000129.3:p.Ala986= |