Linked Data
MyVariant Identifiers:
chr4:g.41747977A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.41745960A>T , CM000666.2:g.41745960A>T | GRCh38 |
| NC_000004.11:g.41747977A>T , CM000666.1:g.41747977A>T | GRCh37 |
| NC_000004.10:g.41442734A>T | NCBI36 |
| NG_008243.1:g.8011T>A , LRG_513:g.8011T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226382.4:c.792T>A MANE Select | ENSP00000226382.2:p.Ala264= | |
| ENST00000226382.3:c.792T>A | ENSP00000226382.2:p.Ala264= | |
| NM_003924.3:c.792T>A , LRG_513t1:c.792T>A | NP_003915.2:p.Ala264= | |
| NM_003924.4:c.792T>A MANE Select | NP_003915.2:p.Ala264= |