Linked Data
MyVariant Identifiers:
chr4:g.52899756C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52033590C>T , CM000666.2:g.52033590C>T | GRCh38 |
| NC_000004.11:g.52899756C>T , CM000666.1:g.52899756C>T | GRCh37 |
| NC_000004.10:g.52594513C>T | NCBI36 |
| NG_008891.1:g.9730G>A , LRG_204:g.9730G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.84G>A MANE Select | ENSP00000370839.6:p.Glu28= | |
| ENST00000381431.9:c.84G>A | ENSP00000370839.5:p.Glu28= | |
| ENST00000506357.5:c.70G>A | ||
| ENST00000514133.1:c.51G>A | ENSP00000425818.1:p.Glu17= | |
| NM_000232.4:c.84G>A , LRG_204t1:c.84G>A | NP_000223.1:p.Glu28= | |
| XM_011534403.1:c.34-3727G>A | XP_011532705.1:n.34-3727G>A | |
| NM_000232.5:c.84G>A MANE Select | NP_000223.1:p.Glu28= |