Linked Data
COSMIC:
COSM6002673
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8012590G>C , CM000679.2:g.8012590G>C | GRCh38 |
| NC_000017.10:g.7915908G>C , CM000679.1:g.7915908G>C | GRCh37 |
| NC_000017.9:g.7856633G>C | NCBI36 |
| NG_009092.1:g.14921G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.2097G>C MANE Select | ENSP00000254854.4:p.Glu699Asp | |
| ENST00000254854.4:c.2097G>C | ENSP00000254854.4:p.Glu699Asp | |
| NM_000180.3:c.2097G>C | NP_000171.1:p.Glu699Asp | |
| XM_011523816.1:c.2097G>C | XP_011522118.1:p.Glu699Asp | |
| NM_000180.4:c.2097G>C MANE Select | NP_000171.1:p.Glu699Asp |