Linked Data
dbSNP Id:
rs1588797039
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.15120338C>T , CM000671.2:g.15120338C>T | GRCh38 |
| NC_000009.11:g.15120336C>T , CM000671.1:g.15120336C>T | GRCh37 |
| NC_000009.10:g.15110336C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000609203.1:n.549+5392G>A |