Linked Data
MyVariant Identifiers:
chr4:g.69535851A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670133A>T , CM000666.2:g.68670133A>T | GRCh38 |
| NC_000004.11:g.69535851A>T , CM000666.1:g.69535851A>T | GRCh37 |
| NC_000004.10:g.69218446A>T | NCBI36 |
| NG_052676.1:g.5644T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.486T>A MANE Select | ENSP00000341045.5:p.Ala162= | |
| ENST00000338206.5:c.486T>A | ENSP00000341045.5:p.Ala162= | |
| ENST00000616841.4:c.486T>A | ENSP00000482004.1:p.Ala162= | |
| NM_001076.3:c.486T>A | NP_001067.2:p.Ala162= | |
| NM_001076.4:c.486T>A MANE Select | NP_001067.2:p.Ala162= |