Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189571727T>G , CM000664.2:g.189571727T>G | GRCh38 |
| NC_000002.11:g.190436453T>G , CM000664.1:g.190436453T>G | GRCh37 |
| NC_000002.10:g.190144698T>G | NCBI36 |
| NG_009027.1:g.14085A>C , LRG_837:g.14085A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.502A>C MANE Select | ENSP00000261024.3:p.Ser168Arg | |
| ENST00000261024.6:c.502A>C | ENSP00000261024.2:p.Ser168Arg | |
| ENST00000427241.5:c.502A>C | ENSP00000390005.1:p.Ser168Arg | |
| NM_014585.5:c.502A>C , LRG_837t1:c.502A>C | NP_055400.1:p.Ser168Arg | |
| XM_005246505.1:c.382A>C | XP_005246562.1:p.Ser128Arg | |
| XM_005246505.2:c.382A>C | XP_005246562.1:p.Ser128Arg | |
| XM_017003938.2:c.382A>C | XP_016859427.1:p.Ser128Arg | |
| NM_014585.6:c.502A>C MANE Select | NP_055400.1:p.Ser168Arg |