Linked Data
dbSNP Id:
rs1847287181
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.10368950T>G , CM000673.2:g.10368950T>G | GRCh38 |
| NC_000011.9:g.10390497T>G , CM000673.1:g.10390497T>G | GRCh37 |
| NC_000011.8:g.10347073T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295663.9:n.51-23332T>G | ||
| ENST00000527261.5:n.501+38241T>G | ||
| ENST00000532250.5:c.-6+38241T>G | ENSP00000432707.1:n.-6+38241T>G | |
| ENST00000532966.1:n.119+11559T>G | ||
| NR_103765.1:n.501+38241T>G |