Linked Data
dbSNP Id:
rs1734040688
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99321851C>A , CM000666.2:g.99321851C>A | GRCh38 |
| NC_000004.11:g.100243008C>A , CM000666.1:g.100243008C>A | GRCh37 |
| NC_000004.10:g.100462031C>A | NCBI36 |
| NG_011435.1:g.4565G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000639454.1:c.19-2965G>T | ENSP00000491622.1:n.19-2965G>T |