Linked Data
dbSNP Id:
rs1577361161
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24794772T>G , CM000666.2:g.24794772T>G | GRCh38 |
| NC_000004.11:g.24796394T>G , CM000666.1:g.24796394T>G | GRCh37 |
| NC_000004.10:g.24405492T>G | NCBI36 |
| NG_012213.1:g.4310T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-17+4670T>G | ENSP00000472134.1:n.-17+4670T>G |