Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.33850968G>T , CM000682.2:g.33850968G>T | GRCh38 |
| NC_000020.10:g.32438774G>T , CM000682.1:g.32438774G>T | GRCh37 |
| NC_000020.9:g.31902435G>T | NCBI36 |
| NG_015820.1:g.44665G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000217402.3:c.385G>T MANE Select | ENSP00000217402.2:p.Asp129Tyr | |
| ENST00000217402.2:c.385G>T | ENSP00000217402.2:p.Asp129Tyr | |
| NM_176812.4:c.385G>T | NP_789782.1:p.Asp129Tyr | |
| NM_176812.5:c.385G>T MANE Select | NP_789782.1:p.Asp129Tyr |