Linked Data
COSMIC:
COSM4966088
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68444637T>C , CM000663.2:g.68444637T>C | GRCh38 |
| NC_000001.10:g.68910320T>C , CM000663.1:g.68910320T>C | GRCh37 |
| NC_000001.9:g.68682908T>C | NCBI36 |
| NG_008472.1:g.10323A>G | |
| NG_008472.2:g.10323A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.389A>G MANE Select | ENSP00000262340.5:p.Asp130Gly | |
| ENST00000262340.5:c.389A>G | ENSP00000262340.5:p.Asp130Gly | |
| NM_000329.2:c.389A>G | NP_000320.1:p.Asp130Gly | |
| XM_017002027.1:c.113A>G | XP_016857516.1:p.Asp38Gly | |
| NM_000329.3:c.389A>G MANE Select | NP_000320.1:p.Asp130Gly |