Linked Data
MyVariant Identifiers:
chr11:g.124742420G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124872524G>T , CM000673.2:g.124872524G>T | GRCh38 |
| NC_000011.9:g.124742420G>T , CM000673.1:g.124742420G>T | GRCh37 |
| NC_000011.8:g.124247630G>T | NCBI36 |
| NG_016214.1:g.12116G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397801.6:c.1302G>T MANE Select | ENSP00000380903.1:p.Leu434= | |
| ENST00000397801.5:c.1302G>T | ENSP00000380903.1:p.Leu434= | |
| ENST00000538940.5:c.1236G>T | ENSP00000441797.1:p.Leu412= | |
| NM_022370.3:c.1302G>T | NP_071765.2:p.Leu434= | |
| XM_011542953.1:c.2274G>T | XP_011541255.1:p.Leu758= | |
| XM_017018122.1:c.1236G>T | XP_016873611.1:p.Leu412= | |
| NM_022370.4:c.1302G>T MANE Select | NP_071765.2:p.Leu434= |