Linked Data
gnomAD v4:
2-189035185-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189035185C>A , CM000664.2:g.189035185C>A | GRCh38 |
| NC_000002.11:g.189899911C>A , CM000664.1:g.189899911C>A | GRCh37 |
| NC_000002.10:g.189608156C>A | NCBI36 |
| NG_011799.1:g.149695G>T | |
| NG_011799.2:g.149695G>T | |
| NG_011799.3:g.195117G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.4114-30G>T MANE Select | ENSP00000364000.3:n.4114-30G>T | |
| ENST00000374866.7:c.4114-30G>T | ENSP00000364000.3:n.4114-30G>T | |
| ENST00000618828.1:c.2953-30G>T | ENSP00000482184.1:n.2953-30G>T | |
| NM_000393.3:c.4114-30G>T | NP_000384.2:n.4114-30G>T | |
| XM_011510573.1:c.3976-30G>T | XP_011508875.1:n.3976-30G>T | |
| NM_000393.4:c.4114-30G>T | NP_000384.2:n.4114-30G>T | |
| XM_011510573.3:c.3976-30G>T | XP_011508875.1:n.3976-30G>T | |
| NM_000393.5:c.4114-30G>T MANE Select | NP_000384.2:n.4114-30G>T |