Linked Data
MyVariant Identifiers:
chr2:g.190428356T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189563630T>A , CM000664.2:g.189563630T>A | GRCh38 |
| NC_000002.11:g.190428356T>A , CM000664.1:g.190428356T>A | GRCh37 |
| NC_000002.10:g.190136601T>A | NCBI36 |
| NG_009027.1:g.22182A>T , LRG_837:g.22182A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.1356A>T MANE Select | ENSP00000261024.3:p.Ile452= | |
| ENST00000261024.6:c.1356A>T | ENSP00000261024.2:p.Ile452= | |
| NM_014585.5:c.1356A>T , LRG_837t1:c.1356A>T | NP_055400.1:p.Ile452= | |
| XM_005246505.1:c.1236A>T | XP_005246562.1:p.Ile412= | |
| XM_005246505.2:c.1236A>T | XP_005246562.1:p.Ile412= | |
| XM_017003938.2:c.1236A>T | XP_016859427.1:p.Ile412= | |
| NM_014585.6:c.1356A>T MANE Select | NP_055400.1:p.Ile452= |