Linked Data
dbSNP Id:
rs1907988920
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.71112671G>T , CM000679.2:g.71112671G>T | GRCh38 |
| NC_000017.10:g.69108812G>T , CM000679.1:g.69108812G>T | GRCh37 |
| NC_000017.9:g.66620407G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_104152.1:n.218-13053C>A |