Linked Data
MyVariant Identifiers:
chr22:g.50659361T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50220932T>G , CM000684.2:g.50220932T>G | GRCh38 |
| NC_000022.10:g.50659361T>G , CM000684.1:g.50659361T>G | GRCh37 |
| NC_000022.9:g.49001488T>G | NCBI36 |
| NG_032160.1:g.29040A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248846.10:c.3427A>C MANE Select | ENSP00000248846.5:p.Arg1143= | |
| ENST00000248846.9:c.3427A>C | ENSP00000248846.5:p.Arg1143= | |
| ENST00000439308.6:c.3427A>C | ENSP00000397387.2:p.Arg1143= | |
| ENST00000491449.5:n.1734A>C | ||
| ENST00000498611.5:n.3617+343A>C | ||
| NM_020461.3:c.3427A>C | NP_065194.2:p.Arg1143= | |
| XR_938347.1:n.3992A>C | ||
| XR_938348.1:n.3050-917A>C | ||
| XR_001755343.2:n.3996A>C | ||
| XR_001755344.2:n.3996A>C | ||
| XR_002958720.1:n.3054-917A>C | ||
| XR_938347.2:n.3996A>C | ||
| NM_020461.4:c.3427A>C MANE Select | NP_065194.3:p.Arg1143= |