Linked Data
MyVariant Identifiers:
chr2:g.190428449G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189563723G>T , CM000664.2:g.189563723G>T | GRCh38 |
| NC_000002.11:g.190428449G>T , CM000664.1:g.190428449G>T | GRCh37 |
| NC_000002.10:g.190136694G>T | NCBI36 |
| NG_009027.1:g.22089C>A , LRG_837:g.22089C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.1263C>A MANE Select | ENSP00000261024.3:p.Thr421= | |
| ENST00000261024.6:c.1263C>A | ENSP00000261024.2:p.Thr421= | |
| NM_014585.5:c.1263C>A , LRG_837t1:c.1263C>A | NP_055400.1:p.Thr421= | |
| XM_005246505.1:c.1143C>A | XP_005246562.1:p.Thr381= | |
| XM_005246505.2:c.1143C>A | XP_005246562.1:p.Thr381= | |
| XM_017003938.2:c.1143C>A | XP_016859427.1:p.Thr381= | |
| NM_014585.6:c.1263C>A MANE Select | NP_055400.1:p.Thr421= |