Linked Data
dbSNP Id:
rs1724945039
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.78667794T>A , CM000666.2:g.78667794T>A | GRCh38 |
| NC_000004.11:g.79588948T>A , CM000666.1:g.79588948T>A | GRCh37 |
| NC_000004.10:g.79807972T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_038303.1:n.473+4783T>A | ||
| NR_038304.1:n.473+4783T>A | ||
| NR_038305.1:n.380-5549T>A | ||
| NR_038306.1:n.380-12967T>A | ||
| NR_038307.1:n.364+4783T>A | ||
| NR_038308.1:n.325+4822T>A |