Linked Data
COSMIC:
COSM6048870
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.31820219C>A , CM000682.2:g.31820219C>A | GRCh38 |
| NC_000020.10:g.30408022C>A , CM000682.1:g.30408022C>A | GRCh37 |
| NC_000020.9:g.29871683C>A | NCBI36 |
| NG_012847.1:g.5845C>A , LRG_392:g.5845C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375985.5:c.146C>A MANE Select | ENSP00000365152.4:p.Thr49Asn | |
| ENST00000375985.4:c.146C>A | ENSP00000365152.4:p.Thr49Asn | |
| ENST00000375994.6:c.146C>A | ENSP00000365162.2:p.Thr49Asn | |
| NM_033118.3:c.146C>A , LRG_392t1:c.146C>A | NP_149109.1:p.Thr49Asn | |
| XR_244155.1:n.311C>A | ||
| NM_033118.4:c.146C>A MANE Select | NP_149109.1:p.Thr49Asn |