Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022450A>C , CM000685.2:g.155022450A>C | GRCh38 |
| NC_000023.10:g.154250725A>C , CM000685.1:g.154250725A>C | GRCh37 |
| NC_000023.9:g.153903919A>C | NCBI36 |
| NG_011403.1:g.5274T>G | |
| NG_011403.2:g.5274T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.103T>G MANE Select | ENSP00000353393.4:p.Tyr35Asp | |
| ENST00000647125.1:c.103T>G | ENSP00000496062.1:p.Tyr35Asp | |
| ENST00000360256.8:c.103T>G | ENSP00000353393.4:p.Tyr35Asp | |
| ENST00000423959.5:c.38+4330T>G | ENSP00000409446.1:n.38+4330T>G | |
| ENST00000453950.1:c.85T>G | ENSP00000389153.1:p.Tyr29Asp | |
| NM_000132.3:c.103T>G | NP_000123.1:p.Tyr35Asp | |
| XM_011531126.1:c.38+4330T>G | XP_011529428.1:n.38+4330T>G | |
| NM_000132.4:c.103T>G MANE Select | NP_000123.1:p.Tyr35Asp |