Linked Data
dbSNP Id:
rs2143599707
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.73811613A>T , CM000679.2:g.73811613A>T | GRCh38 |
| NC_000017.10:g.71807752A>T , CM000679.1:g.71807752A>T | GRCh37 |
| NC_000017.9:g.69319347A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_027146.1:n.228+12075T>A |