Linked Data
dbSNP Id:
rs1288076667
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.53824004A>T , CM000676.2:g.53824004A>T | GRCh38 |
| NC_000014.8:g.54290722A>T , CM000676.1:g.54290722A>T | GRCh37 |
| NC_000014.7:g.53360472A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943872.1:n.392+25718T>A | ||
| XR_943873.1:n.299+25811T>A | ||
| XR_943874.1:n.392+25718T>A | ||
| XR_943875.1:n.392+25718T>A | ||
| XR_943878.1:n.330-50500A>T | ||
| XR_001750967.2:n.416+25718T>A | ||
| XR_001750968.1:n.324+25811T>A | ||
| XR_943872.3:n.415+25718T>A | ||
| XR_943873.2:n.322+25811T>A | ||
| XR_943874.3:n.419+25718T>A |