Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46010966G>T , CM000682.2:g.46010966G>T | GRCh38 |
| NC_000020.10:g.44639605G>T , CM000682.1:g.44639605G>T | GRCh37 |
| NC_000020.9:g.44073012G>T | NCBI36 |
| NG_011468.1:g.7059G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.565G>T MANE Select | ENSP00000361405.3:p.Ala189Ser | |
| NM_004994.2:c.565G>T | NP_004985.2:p.Ala189Ser | |
| NM_004994.3:c.565G>T MANE Select | NP_004985.2:p.Ala189Ser |