Linked Data
MyVariant Identifiers:
chr15:g.75042562G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74750221G>T , CM000677.2:g.74750221G>T | GRCh38 |
| NC_000015.9:g.75042562G>T , CM000677.1:g.75042562G>T | GRCh37 |
| NC_000015.8:g.72829615G>T | NCBI36 |
| NG_008431.1:g.32680G>T | |
| NG_008431.2:g.32680G>T | |
| NG_061543.1:g.6377G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.483G>T MANE Select | ENSP00000342007.4:p.Leu161= | |
| ENST00000343932.4:c.483G>T | ENSP00000342007.4:p.Leu161= | |
| NM_000761.4:c.483G>T | NP_000752.2:p.Leu161= | |
| NM_000761.5:c.483G>T MANE Select | NP_000752.2:p.Leu161= |