Linked Data
MyVariant Identifiers:
chr10:g.124266209C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506693C>T , CM000672.2:g.122506693C>T | GRCh38 |
| NC_000010.10:g.124266209C>T , CM000672.1:g.124266209C>T | GRCh37 |
| NC_000010.9:g.124256199C>T | NCBI36 |
| NG_011554.1:g.50169C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.780C>T MANE Select | ENSP00000357980.3:p.Gly260= | |
| ENST00000648167.1:c.462C>T | ENSP00000498033.1:p.Gly154= | |
| ENST00000368984.7:c.780C>T | ENSP00000357980.3:p.Gly260= | |
| ENST00000420892.1:c.3C>T | ENSP00000412676.1:p.Gly1= | |
| NM_002775.4:c.780C>T | NP_002766.1:p.Gly260= | |
| NM_002775.5:c.780C>T MANE Select | NP_002766.1:p.Gly260= |