Linked Data
MyVariant Identifiers:
chr2:g.190428866A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189564140A>C , CM000664.2:g.189564140A>C | GRCh38 |
| NC_000002.11:g.190428866A>C , CM000664.1:g.190428866A>C | GRCh37 |
| NC_000002.10:g.190137111A>C | NCBI36 |
| NG_009027.1:g.21672T>G , LRG_837:g.21672T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.846T>G MANE Select | ENSP00000261024.3:p.Pro282= | |
| ENST00000261024.6:c.846T>G | ENSP00000261024.2:p.Pro282= | |
| NM_014585.5:c.846T>G , LRG_837t1:c.846T>G | NP_055400.1:p.Pro282= | |
| XM_005246505.1:c.726T>G | XP_005246562.1:p.Pro242= | |
| XM_005246505.2:c.726T>G | XP_005246562.1:p.Pro242= | |
| XM_017003938.2:c.726T>G | XP_016859427.1:p.Pro242= | |
| NM_014585.6:c.846T>G MANE Select | NP_055400.1:p.Pro282= |