Linked Data
dbSNP Id:
rs1009200362
gnomAD v4:
10-88934958-T-C
MyVariant Identifiers:
chr10:g.90694715T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.88934958T>C , CM000672.2:g.88934958T>C | GRCh38 |
| NC_000010.10:g.90694715T>C , CM000672.1:g.90694715T>C | GRCh37 |
| NC_000010.9:g.90684695T>C | NCBI36 |
| NG_011541.1:g.61433A>G , LRG_781:g.61433A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371927.7:c.1254+12522T>C (STAMBPL1) | ENSP00000360995.3:n.1254+12522T>C | |
| NR_125373.1:n.583T>C (ACTA2-AS1) |