MyVariant.info:
GRCh37
chr11:g.4159457A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.4138227A>T , CM000673.2:g.4138227A>T | GRCh38 |
| NC_000011.9:g.4159457A>T , CM000673.1:g.4159457A>T | GRCh37 |
| NC_000011.8:g.4116033A>T | NCBI36 |
| NG_027992.2:g.48534A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300738.10:c.2223A>T MANE Select | ENSP00000300738.5:p.Thr741= | |
| ENST00000300738.9:c.2223A>T | ENSP00000300738.5:p.Thr741= | |
| ENST00000532170.5:c.*2099A>T | ENSP00000435656.1:n.*2099A>T | |
| ENST00000533349.5:c.*1931A>T | ENSP00000434069.1:n.*1931A>T | |
| ENST00000533495.5:c.*1371A>T | ENSP00000436377.1:n.*1371A>T | |
| ENST00000534285.5:c.1557A>T | ENSP00000431464.1:p.Thr519= | |
| NM_001033.3:c.2223A>T | NP_001024.1:p.Thr741= | |
| XM_011520277.1:c.1932A>T | XP_011518579.1:p.Thr644= | |
| XM_011520278.1:c.1557A>T | XP_011518580.1:p.Thr519= | |
| XM_011520279.1:c.1209A>T | XP_011518581.1:p.Thr403= | |
| NM_001033.4:c.2223A>T | NP_001024.1:p.Thr741= | |
| NM_001318064.1:c.1932A>T | NP_001304993.1:p.Thr644= | |
| NM_001318065.1:c.1209A>T | NP_001304994.1:p.Thr403= | |
| NM_001330193.1:c.1557A>T | NP_001317122.1:p.Thr519= | |
| NM_001033.5:c.2223A>T MANE Select | NP_001024.1:p.Thr741= |