Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124382T>C , CM000664.2:g.71124382T>C | GRCh38 |
| NC_000002.11:g.71351512T>C , CM000664.1:g.71351512T>C | GRCh37 |
| NC_000002.10:g.71205020T>C | NCBI36 |
| NG_008977.1:g.10883A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.202A>G MANE Select | ENSP00000244217.5:p.Ile68Val | |
| ENST00000244217.5:c.202A>G | ENSP00000244217.5:p.Ile68Val | |
| ENST00000413592.5:c.70A>G | ENSP00000391140.1:p.Ile24Val | |
| ENST00000486135.1:c.-84A>G | ENSP00000441569.1:n.-84A>G | |
| ENST00000494660.6:c.-84A>G | ENSP00000437361.1:n.-84A>G | |
| NM_032601.3:c.202A>G | NP_115990.3:p.Ile68Val | |
| XM_005264613.2:c.202A>G | XP_005264670.1:p.Ile68Val | |
| XR_939729.1:n.271A>G | ||
| XR_939729.2:n.271A>G | ||
| NM_032601.4:c.202A>G MANE Select | NP_115990.3:p.Ile68Val |