Linked Data
gnomAD v4:
2-189058890-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189058890C>T , CM000664.2:g.189058890C>T | GRCh38 |
| NC_000002.11:g.189923616C>T , CM000664.1:g.189923616C>T | GRCh37 |
| NC_000002.10:g.189631861C>T | NCBI36 |
| NG_011799.1:g.125990G>A | |
| NG_011799.2:g.125990G>A | |
| NG_011799.3:g.171412G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2089G>A MANE Select | ENSP00000364000.3:p.Val697Ile | |
| ENST00000374866.7:c.2089G>A | ENSP00000364000.3:p.Val697Ile | |
| ENST00000470524.2:n.195G>A | ||
| ENST00000618828.1:c.928G>A | ENSP00000482184.1:p.Val310Ile | |
| NM_000393.3:c.2089G>A | NP_000384.2:p.Val697Ile | |
| XM_011510573.1:c.1951G>A | XP_011508875.1:p.Val651Ile | |
| NM_000393.4:c.2089G>A | NP_000384.2:p.Val697Ile | |
| XM_011510573.3:c.1951G>A | XP_011508875.1:p.Val651Ile | |
| NM_000393.5:c.2089G>A MANE Select | NP_000384.2:p.Val697Ile |