Linked Data
ClinVar Variation Id:
298437
dbSNP Id:
rs717620
ExAC:
10:101542578 C / T
gnomAD v2:
10-101542578-C-T
gnomAD v3:
10-99782821-C-T
gnomAD v4:
10-99782821-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99782821C>T , CM000672.2:g.99782821C>T | GRCh38 |
| NC_000010.10:g.101542578C>T , CM000672.1:g.101542578C>T | GRCh37 |
| NC_000010.9:g.101532568C>T | NCBI36 |
| NG_011798.1:g.5116C>T | |
| NG_011798.2:g.5224C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647814.1:c.-24C>T MANE Select | ENSP00000497274.1:n.-24C>T | |
| ENST00000647836.1:n.182C>T | ||
| ENST00000648324.1:c.-24C>T | ENSP00000497248.1:n.-24C>T | |
| ENST00000648689.1:c.-24C>T | ENSP00000496972.1:n.-24C>T | |
| ENST00000649493.1:c.-24C>T | ENSP00000496847.1:n.-24C>T | |
| ENST00000649932.1:c.-24C>T | ENSP00000498120.1:n.-24C>T | |
| ENST00000370434.1:c.-24C>T | ENSP00000359463.1:n.-24C>T | |
| ENST00000370449.8:c.-24C>T | ENSP00000359478.4:n.-24C>T | |
| NM_000392.4:c.-24C>T | NP_000383.1:n.-24C>T | |
| XM_006717631.2:c.-24C>T | XP_006717694.1:n.-24C>T | |
| XM_011539291.1:c.-24C>T | XP_011537593.1:n.-24C>T | |
| XR_945604.1:n.166C>T | ||
| XR_945605.1:n.168C>T | ||
| NM_000392.5:c.-24C>T MANE Select | NP_000383.2:n.-24C>T | |
| XM_006717631.4:c.-24C>T | XP_006717694.1:n.-24C>T | |
| XM_011539291.3:c.-24C>T | XP_011537593.1:n.-24C>T | |
| XM_017015675.2:c.-24C>T | XP_016871164.1:n.-24C>T | |
| XR_945604.3:n.220C>T | ||
| XR_945605.3:n.220C>T |