Linked Data
ClinVar Variation Id:
580934
ClinVar RCV Id:
RCV000704612
dbSNP Id:
rs1490895935
gnomAD v4:
19-33302122-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33302122G>A , CM000681.2:g.33302122G>A | GRCh38 |
| NC_000019.9:g.33793028G>A , CM000681.1:g.33793028G>A | GRCh37 |
| NC_000019.8:g.38484868G>A | NCBI36 |
| NG_012022.1:g.5403C>T , LRG_456:g.5403C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000498907.3:c.293C>T MANE Select | ENSP00000427514.1:p.Thr98Met | |
| ENST00000498907.2:c.293C>T | ENSP00000427514.1:p.Thr98Met | |
| NM_001285829.1:c.-65C>T | NP_001272758.1:n.-65C>T | |
| NM_001287424.1:c.398C>T | NP_001274353.1:p.Thr133Met | |
| NM_001287435.1:c.251C>T | NP_001274364.1:p.Thr84Met | |
| NM_004364.4:c.293C>T | NP_004355.2:p.Thr98Met | |
| NM_001287424.2:c.398C>T | NP_001274353.1:p.Thr133Met | |
| NM_004364.5:c.293C>T MANE Select | NP_004355.2:p.Thr98Met | |
| NM_001285829.2:c.-65C>T | NP_001272758.1:n.-65C>T | |
| NM_001287435.2:c.251C>T | NP_001274364.1:p.Thr84Met |