Linked Data
MyVariant Identifiers:
chr15:g.74631942G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74339601G>A , CM000677.2:g.74339601G>A | GRCh38 |
| NC_000015.9:g.74631942G>A , CM000677.1:g.74631942G>A | GRCh37 |
| NC_000015.8:g.72418995G>A | NCBI36 |
| NG_007973.1:g.33141C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268053.11:c.1143C>T MANE Select | ENSP00000268053.6:p.Ile381= | |
| ENST00000268053.10:c.1143C>T | ENSP00000268053.6:p.Ile381= | |
| ENST00000358632.8:c.669C>T | ENSP00000351455.4:p.Ile223= | |
| ENST00000435365.5:c.1143C>T | ENSP00000391081.1:p.Ile381= | |
| ENST00000566674.5:c.669C>T | ENSP00000456941.1:p.Ile223= | |
| NM_000781.2:c.1143C>T | NP_000772.2:p.Ile381= | |
| NM_001099773.1:c.669C>T | NP_001093243.1:p.Ile223= | |
| NM_000781.3:c.1143C>T MANE Select | NP_000772.2:p.Ile381= | |
| NM_001099773.2:c.669C>T | NP_001093243.1:p.Ile223= |