Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150977867T>A , CM000669.2:g.150977867T>A | GRCh38 |
| NC_000007.13:g.150674955T>A , CM000669.1:g.150674955T>A | GRCh37 |
| NC_000007.12:g.150305888T>A | NCBI36 |
| NG_008916.1:g.5060A>T , LRG_288:g.5060A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262186.10:c.47A>T MANE Select | ENSP00000262186.5:p.Asp16Val | |
| ENST00000262186.9:c.47A>T | ENSP00000262186.5:p.Asp16Val | |
| ENST00000430723.4:c.-131A>T | ENSP00000387657.4:n.-131A>T | |
| ENST00000532957.5:n.270A>T | ||
| NM_000238.3:c.47A>T , LRG_288t1:c.47A>T | NP_000229.1:p.Asp16Val | |
| NM_172056.2:c.47A>T , LRG_288t2:c.47A>T | NP_742053.1:p.Asp16Val | |
| XM_011516186.1:c.47A>T | XP_011514488.1:p.Asp16Val | |
| XM_011516186.3:c.47A>T | XP_011514488.1:p.Asp16Val | |
| NM_000238.4:c.47A>T MANE Select | NP_000229.1:p.Asp16Val |