Linked Data
MyVariant Identifiers:
chr4:g.52894248G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028082G>T , CM000666.2:g.52028082G>T | GRCh38 |
| NC_000004.11:g.52894248G>T , CM000666.1:g.52894248G>T | GRCh37 |
| NC_000004.10:g.52589005G>T | NCBI36 |
| NG_008891.1:g.15238C>A , LRG_204:g.15238C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.639C>A MANE Select | ENSP00000370839.6:p.Thr213= | |
| ENST00000381431.9:c.639C>A | ENSP00000370839.5:p.Thr213= | |
| NM_000232.4:c.639C>A , LRG_204t1:c.639C>A | NP_000223.1:p.Thr213= | |
| XM_006714049.2:c.342C>A | XP_006714112.1:p.Thr114= | |
| XM_011534403.1:c.429C>A | XP_011532705.1:p.Thr143= | |
| XM_011534404.1:c.342C>A | XP_011532706.1:p.Thr114= | |
| NM_000232.5:c.639C>A MANE Select | NP_000223.1:p.Thr213= |