Linked Data
dbSNP Id:
rs1764549559
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24491205G>C , CM000668.2:g.24491205G>C | GRCh38 |
| NC_000006.11:g.24491433G>C , CM000668.1:g.24491433G>C | GRCh37 |
| NC_000006.10:g.24599412G>C | NCBI36 |
| NG_008161.1:g.1237G>C | |
| NG_029888.2:g.3418C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474784.5:n.240-1708C>G | ||
| ENST00000475417.1:n.234-1708C>G | ||
| XM_011514509.1:c.45-1708C>G | XP_011512811.1:n.45-1708C>G | |
| XM_017010753.2:c.45-1708C>G | XP_016866242.1:n.45-1708C>G | |
| XR_002956277.1:n.267-1708C>G |