Linked Data
gnomAD v4:
2-189050576-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189050576C>T , CM000664.2:g.189050576C>T | GRCh38 |
| NC_000002.11:g.189915302C>T , CM000664.1:g.189915302C>T | GRCh37 |
| NC_000002.10:g.189623547C>T | NCBI36 |
| NG_011799.1:g.134304G>A | |
| NG_011799.2:g.134304G>A | |
| NG_011799.3:g.179726G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.3032G>A MANE Select | ENSP00000364000.3:p.Gly1011Asp | |
| ENST00000374866.7:c.3032G>A | ENSP00000364000.3:p.Gly1011Asp | |
| ENST00000618828.1:c.1871G>A | ENSP00000482184.1:p.Gly624Asp | |
| NM_000393.3:c.3032G>A | NP_000384.2:p.Gly1011Asp | |
| XM_011510573.1:c.2894G>A | XP_011508875.1:p.Gly965Asp | |
| NM_000393.4:c.3032G>A | NP_000384.2:p.Gly1011Asp | |
| XM_011510573.3:c.2894G>A | XP_011508875.1:p.Gly965Asp | |
| NM_000393.5:c.3032G>A MANE Select | NP_000384.2:p.Gly1011Asp |