Linked Data
MyVariant Identifiers:
chr11:g.6340714T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319484T>C , CM000673.2:g.6319484T>C | GRCh38 |
| NC_000011.9:g.6340714T>C , CM000673.1:g.6340714T>C | GRCh37 |
| NC_000011.8:g.6297290T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.465A>G MANE Select | ENSP00000307292.3:p.Pro155= | |
| ENST00000303927.3:c.465A>G | ENSP00000307292.3:p.Pro155= | |
| ENST00000524852.1:n.251A>G | ||
| ENST00000530979.1:c.561A>G | ENSP00000432047.1:p.Pro187= | |
| ENST00000532354.1:n.487A>G | ||
| NM_145040.2:c.465A>G | NP_659477.2:p.Pro155= | |
| XR_930997.1:n.720+1264T>C | ||
| XR_001748106.1:n.95T>C | ||
| XR_242848.4:n.344T>C | ||
| NM_145040.3:c.465A>G MANE Select | NP_659477.2:p.Pro155= |