Linked Data
ClinVar Variation Id:
333126
dbSNP Id:
rs7586
gnomAD v2:
2-189898498-C-T
gnomAD v3:
2-189033772-C-T
gnomAD v4:
2-189033772-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189033772C>T , CM000664.2:g.189033772C>T | GRCh38 |
| NC_000002.11:g.189898498C>T , CM000664.1:g.189898498C>T | GRCh37 |
| NC_000002.10:g.189606743C>T | NCBI36 |
| NG_011799.1:g.151108G>A | |
| NG_011799.2:g.151108G>A | |
| NG_011799.3:g.196530G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.*298G>A MANE Select | ENSP00000364000.3:n.*298G>A | |
| ENST00000374866.7:c.*298G>A | ENSP00000364000.3:n.*298G>A | |
| ENST00000618828.1:c.*298G>A | ENSP00000482184.1:n.*298G>A | |
| NM_000393.3:c.*298G>A | NP_000384.2:n.*298G>A | |
| XM_011510573.1:c.*298G>A | XP_011508875.1:n.*298G>A | |
| NM_000393.4:c.*298G>A | NP_000384.2:n.*298G>A | |
| XM_011510573.3:c.*298G>A | XP_011508875.1:n.*298G>A | |
| NM_000393.5:c.*298G>A MANE Select | NP_000384.2:n.*298G>A |