Linked Data
MyVariant Identifiers:
chr10:g.96534952G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775195G>T , CM000672.2:g.94775195G>T | GRCh38 |
| NC_000010.10:g.96534952G>T , CM000672.1:g.96534952G>T | GRCh37 |
| NC_000010.9:g.96524942G>T | NCBI36 |
| NG_008384.2:g.17490G>T | |
| NG_008384.3:g.17515G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.306G>T MANE Select | ENSP00000360372.3:p.Leu102= | |
| ENST00000645461.1:n.1359G>T | ||
| ENST00000371321.7:c.306G>T | ENSP00000360372.3:p.Leu102= | |
| ENST00000464755.1:c.1069G>T | ENSP00000483243.1:n.1069G>T | |
| ENST00000480405.2:c.306G>T | ENSP00000483847.1:p.Leu102= | |
| NM_000769.2:c.306G>T | NP_000760.1:p.Leu102= | |
| NM_000769.4:c.306G>T MANE Select | NP_000760.1:p.Leu102= |