Linked Data
dbSNP Id:
rs10758593
gnomAD v2:
9-4292083-G-A
gnomAD v3:
9-4292083-G-A
gnomAD v4:
9-4292083-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4292083G>A , CM000671.2:g.4292083G>A | GRCh38 |
| NC_000009.11:g.4292083G>A , CM000671.1:g.4292083G>A | GRCh37 |
| NC_000009.10:g.4282083G>A | NCBI36 |
| NG_011782.1:g.12953C>T | |
| NG_011782.2:g.12953C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000491889.6:c.-98-5560C>T | ENSP00000419914.1:n.-98-5560C>T | |
| ENST00000682749.1:c.-78+7338C>T | ENSP00000507306.1:n.-78+7338C>T | |
| ENST00000381971.8:c.-98-5560C>T MANE Select | ENSP00000371398.3:n.-98-5560C>T | |
| ENST00000381971.7:c.-98-5560C>T | ENSP00000371398.3:n.-98-5560C>T | |
| ENST00000465708.5:n.497-5560C>T | ||
| ENST00000471664.1:n.585-5560C>T | ||
| ENST00000477901.5:c.-98-5560C>T | ENSP00000417794.1:n.-98-5560C>T | |
| ENST00000478844.5:c.-78+6301C>T | ENSP00000418005.1:n.-78+6301C>T | |
| ENST00000481827.5:c.-98-5560C>T | ENSP00000417883.1:n.-98-5560C>T | |
| ENST00000490709.1:n.416+7338C>T | ||
| ENST00000491889.5:c.-98-5560C>T | ENSP00000419914.1:n.-98-5560C>T | |
| NM_001042413.1:c.-98-5560C>T | NP_001035878.1:n.-98-5560C>T | |
| XM_005251386.3:c.-78+7338C>T | XP_005251443.1:n.-78+7338C>T | |
| XM_005251387.3:c.-556-5560C>T | XP_005251444.1:n.-556-5560C>T | |
| XM_005251388.3:c.-71+7338C>T | XP_005251445.1:n.-71+7338C>T | |
| XM_005251389.3:c.-98-5560C>T | XP_005251446.1:n.-98-5560C>T | |
| XM_006716731.2:c.-98-5560C>T | XP_006716794.1:n.-98-5560C>T | |
| XM_011517763.1:c.-98-5560C>T | XP_011516065.1:n.-98-5560C>T | |
| XM_011517764.1:c.-98-5560C>T | XP_011516066.1:n.-98-5560C>T | |
| XM_011517765.1:c.-98-5560C>T | XP_011516067.1:n.-98-5560C>T | |
| XM_011517767.1:c.-556-5560C>T | XP_011516069.1:n.-556-5560C>T | |
| XM_011517768.1:c.-98-5560C>T | XP_011516070.1:n.-98-5560C>T | |
| XM_011517769.1:c.-98-5560C>T | XP_011516071.1:n.-98-5560C>T | |
| XR_929206.1:n.669-5560C>T | ||
| XM_005251386.4:c.-78+7338C>T | XP_005251443.1:n.-78+7338C>T | |
| XM_005251387.4:c.-556-5560C>T | XP_005251444.1:n.-556-5560C>T | |
| XM_005251388.4:c.-71+7338C>T | XP_005251445.1:n.-71+7338C>T | |
| XM_005251389.5:c.-98-5560C>T | XP_005251446.1:n.-98-5560C>T | |
| XM_006716731.3:c.-98-5560C>T | XP_006716794.1:n.-98-5560C>T | |
| XM_011517763.2:c.-98-5560C>T | XP_011516065.1:n.-98-5560C>T | |
| XM_011517764.2:c.-98-5560C>T | XP_011516066.1:n.-98-5560C>T | |
| XM_011517765.2:c.-98-5560C>T | XP_011516067.1:n.-98-5560C>T | |
| XM_011517767.3:c.-556-5560C>T | XP_011516069.1:n.-556-5560C>T | |
| XM_011517769.2:c.-98-5560C>T | XP_011516071.1:n.-98-5560C>T | |
| XR_929206.2:n.665-5560C>T | ||
| NM_001042413.2:c.-98-5560C>T MANE Select | NP_001035878.1:n.-98-5560C>T |