Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104789T>G , CM000684.2:g.32104789T>G | GRCh38 |
| NC_000022.10:g.32500776T>G , CM000684.1:g.32500776T>G | GRCh37 |
| NC_000022.9:g.30830776T>G | NCBI36 |
| NG_017045.1:g.66758T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1669T>G MANE Select | ENSP00000266088.4:p.Tyr557Asp | |
| ENST00000266088.8:c.1669T>G | ENSP00000266088.4:p.Tyr557Asp | |
| ENST00000543737.2:c.1288T>G | ENSP00000444898.1:p.Tyr430Asp | |
| NM_000343.3:c.1669T>G | NP_000334.1:p.Tyr557Asp | |
| NM_001256314.1:c.1288T>G | NP_001243243.1:p.Tyr430Asp | |
| XR_938173.1:n.591+2049A>C | ||
| XR_938174.1:n.486+15066A>C | ||
| NM_000343.4:c.1669T>G MANE Select | NP_000334.1:p.Tyr557Asp | |
| NM_001256314.2:c.1288T>G | NP_001243243.1:p.Tyr430Asp |