Linked Data
MyVariant Identifiers:
chr4:g.69535857T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670139T>A , CM000666.2:g.68670139T>A | GRCh38 |
| NC_000004.11:g.69535857T>A , CM000666.1:g.69535857T>A | GRCh37 |
| NC_000004.10:g.69218452T>A | NCBI36 |
| NG_052676.1:g.5638A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.480A>T MANE Select | ENSP00000341045.5:p.Leu160= | |
| ENST00000338206.5:c.480A>T | ENSP00000341045.5:p.Leu160= | |
| ENST00000616841.4:c.480A>T | ENSP00000482004.1:p.Leu160= | |
| NM_001076.3:c.480A>T | NP_001067.2:p.Leu160= | |
| NM_001076.4:c.480A>T MANE Select | NP_001067.2:p.Leu160= |