Linked Data
COSMIC:
COSM6279089
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601669G>A , CM000672.2:g.110601669G>A | GRCh38 |
| NC_000010.10:g.112361427G>A , CM000672.1:g.112361427G>A | GRCh37 |
| NC_000010.9:g.112351417G>A | NCBI36 |
| NG_012217.1:g.38979G>A , LRG_774:g.38979G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4910G>A | ||
| ENST00000685743.1:n.2385G>A | ||
| ENST00000686057.1:n.1028G>A | ||
| ENST00000689321.1:n.1640G>A | ||
| ENST00000689986.1:n.466G>A | ||
| ENST00000361804.5:c.2677G>A MANE Select | ENSP00000354720.5:p.Gly893Arg | |
| ENST00000361804.4:c.2677G>A | ENSP00000354720.4:p.Gly893Arg | |
| NM_005445.3:c.2677G>A , LRG_774t1:c.2677G>A | NP_005436.1:p.Gly893Arg | |
| NM_005445.4:c.2677G>A MANE Select | NP_005436.1:p.Gly893Arg |