Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.29917503A>T , CM000685.2:g.29917503A>T | GRCh38 |
| NC_000023.10:g.29935620A>T , CM000685.1:g.29935620A>T | GRCh37 |
| NC_000023.9:g.29845541A>T | NCBI36 |
| NG_008292.1:g.1334940A>T | |
| NG_008292.2:g.1334940A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378993.6:c.818A>T MANE Select | ENSP00000368278.1:p.Tyr273Phe | |
| ENST00000302196.5:c.41A>T | ENSP00000305200.5:p.Tyr14Phe | |
| ENST00000378993.5:c.818A>T | ENSP00000368278.1:p.Tyr273Phe | |
| NM_014271.3:c.818A>T | NP_055086.1:p.Tyr273Phe | |
| XM_005274441.1:c.818A>T | XP_005274498.1:p.Tyr273Phe | |
| XM_011545445.1:c.818A>T | XP_011543747.1:p.Tyr273Phe | |
| XM_017029240.1:c.818A>T | XP_016884729.1:p.Tyr273Phe | |
| XM_017029241.1:c.440A>T | XP_016884730.1:p.Tyr147Phe | |
| NM_014271.4:c.818A>T MANE Select | NP_055086.1:p.Tyr273Phe |