Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.74920190T>A , CM000679.2:g.74920190T>A | GRCh38 |
| NC_000017.10:g.72916285T>A , CM000679.1:g.72916285T>A | GRCh37 |
| NC_000017.9:g.70427880T>A | NCBI36 |
| NG_007882.1:g.8067A>T | |
| NG_033062.1:g.916T>A | |
| NG_007882.2:g.8074A>T | |
| NG_033062.2:g.916T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614341.5:c.646A>T MANE Select | ENSP00000480279.1:p.Met216Leu | |
| ENST00000579243.1:c.*245A>T | ENSP00000462568.1:n.*245A>T | |
| ENST00000614341.4:c.646A>T | ENSP00000480279.1:p.Met216Leu | |
| NM_001282489.2:c.337A>T | NP_001269418.1:p.Met113Leu | |
| NM_173477.4:c.646A>T | NP_775748.2:p.Met216Leu | |
| XM_011524296.1:c.337A>T | XP_011522598.1:p.Met113Leu | |
| XM_011524296.2:c.337A>T | XP_011522598.1:p.Met113Leu | |
| NM_173477.5:c.646A>T MANE Select | NP_775748.2:p.Met216Leu | |
| NM_001282489.3:c.337A>T | NP_001269418.1:p.Met113Leu |