Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.98186922T>C , CM000669.2:g.98186922T>C | GRCh38 |
| NC_000007.13:g.97816234T>C , CM000669.1:g.97816234T>C | GRCh37 |
| NC_000007.12:g.97654170T>C | NCBI36 |
| NG_013375.1:g.85038T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297293.6:c.922T>C MANE Select | ENSP00000297293.5:p.Trp308Arg | |
| ENST00000297293.5:c.922T>C | ENSP00000297293.5:p.Trp308Arg | |
| NM_014916.3:c.922T>C | NP_055731.2:p.Trp308Arg | |
| XM_011515981.1:c.916T>C | XP_011514283.1:p.Trp306Arg | |
| XM_011515981.3:c.916T>C | XP_011514283.1:p.Trp306Arg | |
| NM_014916.4:c.922T>C MANE Select | NP_055731.2:p.Trp308Arg |