Linked Data
MyVariant Identifiers:
chr20:g.48522396G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.49905859G>A , CM000682.2:g.49905859G>A | GRCh38 |
| NC_000020.10:g.48522396G>A , CM000682.1:g.48522396G>A | GRCh37 |
| NC_000020.9:g.47955803G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289431.10:c.1323C>T MANE Select | ENSP00000289431.5:p.Asp441= | |
| ENST00000289431.9:c.1323C>T | ENSP00000289431.5:p.Asp441= | |
| ENST00000422556.1:c.1323C>T | ENSP00000416799.1:p.Asp441= | |
| NM_001135773.1:c.1323C>T | NP_001129245.1:p.Asp441= | |
| NM_006038.3:c.1323C>T | NP_006029.1:p.Asp441= | |
| XM_006723894.1:c.1323C>T | XP_006723957.1:p.Asp441= | |
| XM_011529116.1:c.1323C>T | XP_011527418.1:p.Asp441= | |
| NM_006038.4:c.1323C>T MANE Select | NP_006029.1:p.Asp441= | |
| NM_001135773.2:c.1323C>T | NP_001129245.1:p.Asp441= |