Linked Data
dbSNP Id:
rs1844380366
gnomAD v4:
10-92419113-G-T
MyVariant Identifiers:
chr10:g.94178870G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92419113G>T , CM000672.2:g.92419113G>T | GRCh38 |
| NC_000010.10:g.94178870G>T , CM000672.1:g.94178870G>T | GRCh37 |
| NC_000010.9:g.94168850G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430958.1:n.447G>T | ||
| NR_038243.2:n.453G>T |