Linked Data
MyVariant Identifiers:
chr10:g.96541598T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781841T>G , CM000672.2:g.94781841T>G | GRCh38 |
| NC_000010.10:g.96541598T>G , CM000672.1:g.96541598T>G | GRCh37 |
| NC_000010.9:g.96531588T>G | NCBI36 |
| NG_008384.2:g.24136T>G | |
| NG_008384.3:g.24161T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.663T>G MANE Select | ENSP00000360372.3:p.Thr221= | |
| ENST00000645461.1:n.1716T>G | ||
| ENST00000371321.7:c.663T>G | ENSP00000360372.3:p.Thr221= | |
| ENST00000464755.1:c.1426T>G | ENSP00000483243.1:n.1426T>G | |
| NM_000769.2:c.663T>G | NP_000760.1:p.Thr221= | |
| NM_000769.4:c.663T>G MANE Select | NP_000760.1:p.Thr221= |