Linked Data
dbSNP Id:
rs1845706046
gnomAD v4:
10-88935032-A-G
MyVariant Identifiers:
chr10:g.90694789A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.88935032A>G , CM000672.2:g.88935032A>G | GRCh38 |
| NC_000010.10:g.90694789A>G , CM000672.1:g.90694789A>G | GRCh37 |
| NC_000010.9:g.90684769A>G | NCBI36 |
| NG_011541.1:g.61359T>C , LRG_781:g.61359T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371927.7:c.1254+12596A>G (STAMBPL1) | ENSP00000360995.3:n.1254+12596A>G | |
| NR_125373.1:n.657A>G (ACTA2-AS1) |