Linked Data
MyVariant Identifiers:
chr15:g.75042460A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750119A>T , CM000677.2:g.74750119A>T | GRCh38 |
| NC_000015.9:g.75042460A>T , CM000677.1:g.75042460A>T | GRCh37 |
| NC_000015.8:g.72829513A>T | NCBI36 |
| NG_008431.1:g.32578A>T | |
| NG_008431.2:g.32578A>T | |
| NG_061543.1:g.6275A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.381A>T MANE Select | ENSP00000342007.4:p.Thr127= | |
| ENST00000343932.4:c.381A>T | ENSP00000342007.4:p.Thr127= | |
| NM_000761.4:c.381A>T | NP_000752.2:p.Thr127= | |
| NM_000761.5:c.381A>T MANE Select | NP_000752.2:p.Thr127= |