Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67066174T>A , CM000677.2:g.67066174T>A | GRCh38 |
| NC_000015.9:g.67358512T>A , CM000677.1:g.67358512T>A | GRCh37 |
| NC_000015.8:g.65145566T>A | NCBI36 |
| NG_011990.1:g.5318T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559460.6:c.-110+2230T>A | ENSP00000453082.2:n.-110+2230T>A | |
| ENST00000560424.2:c.20T>A | ENSP00000455540.2:p.Phe7Tyr | |
| ENST00000327367.9:c.20T>A MANE Select | ENSP00000332973.4:p.Phe7Tyr | |
| ENST00000327367.8:c.20T>A | ENSP00000332973.4:p.Phe7Tyr | |
| ENST00000559460.5:c.-110+2230T>A | ENSP00000453082.1:n.-110+2230T>A | |
| NM_005902.3:c.20T>A | NP_005893.1:p.Phe7Tyr | |
| XM_011521559.1:c.20T>A | XP_011519861.1:p.Phe7Tyr | |
| XM_011521559.3:c.20T>A | XP_011519861.1:p.Phe7Tyr | |
| NM_005902.4:c.20T>A MANE Select | NP_005893.1:p.Phe7Tyr |