Linked Data
COSMIC:
COSM1700321
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86671001A>G , CM000670.2:g.86671001A>G | GRCh38 |
| NC_000008.10:g.87683229A>G , CM000670.1:g.87683229A>G | GRCh37 |
| NC_000008.9:g.87752345A>G | NCBI36 |
| NG_016980.1:g.77675T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.436T>C MANE Select | ENSP00000316605.5:p.Tyr146His | |
| ENST00000680314.1:n.197T>C | ||
| ENST00000681746.1:c.436T>C | ENSP00000505959.1:p.Tyr146His | |
| ENST00000320005.5:c.436T>C | ENSP00000316605.5:p.Tyr146His | |
| NM_019098.4:c.436T>C | NP_061971.3:p.Tyr146His | |
| XM_011517138.1:c.22T>C | XP_011515440.1:p.Tyr8His | |
| XM_011517138.2:c.22T>C | XP_011515440.1:p.Tyr8His | |
| NM_019098.5:c.436T>C MANE Select | NP_061971.3:p.Tyr146His |