Linked Data
MyVariant Identifiers:
chr11:g.6340513C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319283C>T , CM000673.2:g.6319283C>T | GRCh38 |
| NC_000011.9:g.6340513C>T , CM000673.1:g.6340513C>T | GRCh37 |
| NC_000011.8:g.6297089C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.666G>A MANE Select | ENSP00000307292.3:p.Pro222= | |
| ENST00000303927.3:c.666G>A | ENSP00000307292.3:p.Pro222= | |
| ENST00000524852.1:n.452G>A | ||
| ENST00000530979.1:c.762G>A | ENSP00000432047.1:p.Pro254= | |
| ENST00000532354.1:n.688G>A | ||
| NM_145040.2:c.666G>A | NP_659477.2:p.Pro222= | |
| XR_930997.1:n.720+1063C>T | ||
| XR_242848.4:n.143C>T | ||
| NM_145040.3:c.666G>A MANE Select | NP_659477.2:p.Pro222= |