Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18672022T>A , CM000685.2:g.18672022T>A | GRCh38 |
| NC_000023.10:g.18690142T>A , CM000685.1:g.18690142T>A | GRCh37 |
| NC_000023.9:g.18600063T>A | NCBI36 |
| NG_008659.3:g.10427A>T , LRG_702:g.10427A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379984.4:c.47A>T MANE Select | ENSP00000369320.3:p.Tyr16Phe | |
| ENST00000379984.3:c.47A>T | ENSP00000369320.3:p.Tyr16Phe | |
| NM_000330.3:c.47A>T , LRG_702t1:c.47A>T | NP_000321.1:p.Tyr16Phe | |
| NM_000330.4:c.47A>T MANE Select | NP_000321.1:p.Tyr16Phe |