Linked Data
COSMIC:
COSM5935574
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942341G>T , CM000672.2:g.94942341G>T | GRCh38 |
| NC_000010.10:g.96702098G>T , CM000672.1:g.96702098G>T | GRCh37 |
| NC_000010.9:g.96692088G>T | NCBI36 |
| NG_008385.1:g.8684G>T | |
| NG_008385.2:g.9184G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.481G>T MANE Select | ENSP00000260682.6:p.Ala161Ser | |
| ENST00000643112.1:c.481G>T | ENSP00000496202.1:p.Ala161Ser | |
| ENST00000645207.1:n.634G>T | ||
| ENST00000260682.6:c.481G>T | ENSP00000260682.6:p.Ala161Ser | |
| ENST00000461906.1:n.506G>T | ||
| ENST00000473496.1:n.252G>T | ||
| NM_000771.3:c.481G>T | NP_000762.2:p.Ala161Ser | |
| NM_000771.4:c.481G>T MANE Select | NP_000762.2:p.Ala161Ser |