Linked Data
ClinVar Variation Id:
42104
ClinVar RCV Id:
RCV000034931
dbSNP Id:
rs111364670
gnomAD v4:
19-38510566-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38510566G>T , CM000681.2:g.38510566G>T | GRCh38 |
| NC_000019.9:g.39001206G>T , CM000681.1:g.39001206G>T | GRCh37 |
| NC_000019.8:g.43693046G>T | NCBI36 |
| NG_008866.1:g.81867G>T , LRG_766:g.81867G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000599547.6:c.9000+1G>T | ENSP00000471601.2:n.9000+1G>T | |
| ENST00000359596.8:c.9000+1G>T MANE Select | ENSP00000352608.2:n.9000+1G>T | |
| ENST00000355481.8:c.9000+1G>T | ENSP00000347667.3:n.9000+1G>T | |
| ENST00000359596.7:c.9000+1G>T | ENSP00000352608.2:n.9000+1G>T | |
| ENST00000360985.7:c.8997+1G>T | ENSP00000354254.4:n.8997+1G>T | |
| ENST00000594335.5:c.2452+1G>T | ||
| NM_000540.2:c.9000+1G>T , LRG_766t1:c.9000+1G>T | NP_000531.2:n.9000+1G>T | |
| NM_001042723.1:c.9000+1G>T | NP_001036188.1:n.9000+1G>T | |
| XM_006723317.1:c.9000+1G>T | XP_006723380.1:n.9000+1G>T | |
| XM_006723319.1:c.9000+1G>T | XP_006723382.1:n.9000+1G>T | |
| XM_011527204.1:c.8997+1G>T | XP_011525506.1:n.8997+1G>T | |
| XM_011527205.1:c.9000+1G>T | XP_011525507.1:n.9000+1G>T | |
| XM_006723317.2:c.9000+1G>T | XP_006723380.1:n.9000+1G>T | |
| XM_006723319.2:c.9000+1G>T | XP_006723382.1:n.9000+1G>T | |
| XM_011527205.2:c.9000+1G>T | XP_011525507.1:n.9000+1G>T | |
| XR_001753735.1:n.9083+1G>T | ||
| NM_000540.3:c.9000+1G>T MANE Select | NP_000531.2:n.9000+1G>T | |
| NM_001042723.2:c.9000+1G>T | NP_001036188.1:n.9000+1G>T |