Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15180133A>T , CM000681.2:g.15180133A>T | GRCh38 |
| NC_000019.9:g.15290944A>T , CM000681.1:g.15290944A>T | GRCh37 |
| NC_000019.8:g.15151944A>T | NCBI36 |
| NG_009819.1:g.25849T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263388.7:c.3266T>A MANE Select | ENSP00000263388.1:p.Leu1089Ter | |
| ENST00000263388.6:c.3266T>A | ENSP00000263388.1:p.Leu1089Ter | |
| ENST00000601011.1:c.3107T>A | ENSP00000473138.1:p.Leu1036Ter | |
| NM_000435.2:c.3266T>A | NP_000426.2:p.Leu1089Ter | |
| XM_005259924.3:c.3110T>A | XP_005259981.1:p.Leu1037Ter | |
| XM_005259924.4:c.3110T>A | XP_005259981.1:p.Leu1037Ter | |
| NM_000435.3:c.3266T>A MANE Select | NP_000426.2:p.Leu1089Ter |