Linked Data
dbSNP Id:
rs1734039584
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99321813A>T , CM000666.2:g.99321813A>T | GRCh38 |
| NC_000004.11:g.100242970A>T , CM000666.1:g.100242970A>T | GRCh37 |
| NC_000004.10:g.100461993A>T | NCBI36 |
| NG_011435.1:g.4603T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000639454.1:c.19-2927T>A | ENSP00000491622.1:n.19-2927T>A |