Linked Data
MyVariant Identifiers:
chr11:g.121177963T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121307254T>G , CM000673.2:g.121307254T>G | GRCh38 |
| NC_000011.9:g.121177963T>G , CM000673.1:g.121177963T>G | GRCh37 |
| NC_000011.8:g.120683173T>G | NCBI36 |
| NG_009446.1:g.19576T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264027.9:c.642T>G MANE Select | ENSP00000264027.4:p.Arg214= | |
| ENST00000264027.8:c.642T>G | ENSP00000264027.4:p.Arg214= | |
| ENST00000392789.2:c.642T>G | ENSP00000376539.2:p.Arg214= | |
| ENST00000527183.1:n.935T>G | ||
| ENST00000528991.1:n.335T>G | ||
| ENST00000534230.5:c.631+11T>G | ENSP00000432550.1:n.631+11T>G | |
| NM_001024956.2:c.642T>G | NP_001020127.1:p.Arg214= | |
| NM_006918.4:c.642T>G | NP_008849.2:p.Arg214= | |
| NM_006918.5:c.642T>G MANE Select | NP_008849.2:p.Arg214= | |
| NM_001024956.3:c.642T>G | NP_001020127.1:p.Arg214= |