Linked Data
ClinVar Variation Id:
256385
ClinVar RCV Id:
RCV000241860
dbSNP Id:
rs886038309
gnomAD v4:
19-38433793-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38433793C>G , CM000681.2:g.38433793C>G | GRCh38 |
| NC_000019.9:g.38924433C>G , CM000681.1:g.38924433C>G | GRCh37 |
| NC_000019.8:g.43616273C>G | NCBI36 |
| NG_008866.1:g.5094C>G , LRG_766:g.5094C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359596.8:c.-37C>G MANE Select | ENSP00000352608.2:n.-37C>G | |
| ENST00000355481.8:c.-37C>G | ENSP00000347667.3:n.-37C>G | |
| ENST00000360985.7:c.-37C>G | ENSP00000354254.4:n.-37C>G | |
| NM_000540.2:c.-37C>G , LRG_766t1:c.-37C>G | NP_000531.2:n.-37C>G | |
| NM_001042723.1:c.-37C>G | NP_001036188.1:n.-37C>G | |
| XM_006723317.1:c.-37C>G | XP_006723380.1:n.-37C>G | |
| XM_006723319.1:c.-37C>G | XP_006723382.1:n.-37C>G | |
| XM_011527204.1:c.-37C>G | XP_011525506.1:n.-37C>G | |
| XM_011527205.1:c.-37C>G | XP_011525507.1:n.-37C>G | |
| XM_006723317.2:c.-37C>G | XP_006723380.1:n.-37C>G | |
| XM_006723319.2:c.-37C>G | XP_006723382.1:n.-37C>G | |
| XM_011527205.2:c.-37C>G | XP_011525507.1:n.-37C>G | |
| XR_001753735.1:n.47C>G | ||
| NM_000540.3:c.-37C>G MANE Select | NP_000531.2:n.-37C>G | |
| NM_001042723.2:c.-37C>G | NP_001036188.1:n.-37C>G |