Linked Data
MyVariant Identifiers:
chr21:g.35742858C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370559C>A , CM000683.2:g.34370559C>A | GRCh38 |
| NC_000021.8:g.35742858C>A , CM000683.1:g.35742858C>A | GRCh37 |
| NC_000021.7:g.34664728C>A | NCBI36 |
| NG_008804.1:g.11536C>A , LRG_291:g.11536C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000290310.4:c.81C>A MANE Select | ENSP00000290310.2:p.Arg27= | |
| ENST00000290310.3:c.81C>A | ENSP00000290310.2:p.Arg27= | |
| NM_172201.1:c.81C>A , LRG_291t1:c.81C>A | NP_751951.1:p.Arg27= | |
| XR_937683.1:n.762G>T | ||
| XR_937684.1:n.762G>T | ||
| XR_001755012.2:n.883G>T | ||
| XR_001755013.2:n.762G>T | ||
| XR_937683.2:n.762G>T | ||
| NM_172201.2:c.81C>A MANE Select | NP_751951.1:p.Arg27= |