Linked Data
dbSNP Id:
rs1873566442
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.19130992T>G , CM000675.2:g.19130992T>G | GRCh38 |
| NC_000013.10:g.19705132T>G , CM000675.1:g.19705132T>G | GRCh37 |
| NC_000013.9:g.18603132T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425713.1:n.493-300T>G |