Linked Data
MyVariant Identifiers:
chr11:g.121177999A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121307290A>T , CM000673.2:g.121307290A>T | GRCh38 |
| NC_000011.9:g.121177999A>T , CM000673.1:g.121177999A>T | GRCh37 |
| NC_000011.8:g.120683209A>T | NCBI36 |
| NG_009446.1:g.19612A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264027.9:c.678A>T MANE Select | ENSP00000264027.4:p.Ser226= | |
| ENST00000264027.8:c.678A>T | ENSP00000264027.4:p.Ser226= | |
| ENST00000392789.2:c.678A>T | ENSP00000376539.2:p.Ser226= | |
| ENST00000527183.1:n.971A>T | ||
| ENST00000534230.5:c.631+47A>T | ENSP00000432550.1:n.631+47A>T | |
| NM_001024956.2:c.678A>T | NP_001020127.1:p.Ser226= | |
| NM_006918.4:c.678A>T | NP_008849.2:p.Ser226= | |
| NM_006918.5:c.678A>T MANE Select | NP_008849.2:p.Ser226= | |
| NM_001024956.3:c.678A>T | NP_001020127.1:p.Ser226= |