Linked Data
MyVariant Identifiers:
chr10:g.90694799G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.88935042G>C , CM000672.2:g.88935042G>C | GRCh38 |
| NC_000010.10:g.90694799G>C , CM000672.1:g.90694799G>C | GRCh37 |
| NC_000010.9:g.90684779G>C | NCBI36 |
| NG_011541.1:g.61349C>G , LRG_781:g.61349C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371927.7:c.1254+12606G>C (STAMBPL1) | ENSP00000360995.3:n.1254+12606G>C | |
| NR_125373.1:n.667G>C (ACTA2-AS1) |