Linked Data
dbSNP Id:
rs975718664
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106940499C>A , CM000685.2:g.106940499C>A | GRCh38 |
| NC_000023.10:g.106183729C>A , CM000685.1:g.106183729C>A | GRCh37 |
| NC_000023.9:g.106070385C>A | NCBI36 |
| NG_016392.1:g.64746G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000604604.1:c.111+52731G>T | ||
| XM_005262190.3:c.*980G>T | XP_005262247.1:n.*980G>T | |
| XM_006724691.2:c.*980G>T | XP_006724754.1:n.*980G>T | |
| XM_011531027.2:c.*980G>T | XP_011529329.1:n.*980G>T | |
| XM_017029844.1:c.*1053G>T | XP_016885333.1:n.*1053G>T |