Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94423117C>T , CM000669.2:g.94423117C>T | GRCh38 |
| NC_000007.13:g.94052429C>T , CM000669.1:g.94052429C>T | GRCh37 |
| NC_000007.12:g.93890365C>T | NCBI36 |
| NG_007405.1:g.33557C>T , LRG_2:g.33557C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.2564C>T MANE Select | ENSP00000297268.6:p.Ala855Val | |
| ENST00000297268.10:c.2564C>T | ENSP00000297268.6:p.Ala855Val | |
| ENST00000481570.5:n.647C>T | ||
| ENST00000497316.5:n.961C>T | ||
| ENST00000620463.1:c.2558C>T | ENSP00000477719.1:p.Ala853Val | |
| NM_000089.3:c.2564C>T , LRG_2t1:c.2564C>T | NP_000080.2:p.Ala855Val | |
| NM_000089.4:c.2564C>T MANE Select | NP_000080.2:p.Ala855Val |