Linked Data
gnomAD v4:
21-44456634-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44456634G>A , CM000683.2:g.44456634G>A | GRCh38 |
| NC_000021.8:g.45876517G>A , CM000683.1:g.45876517G>A | GRCh37 |
| NC_000021.7:g.44700945G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291592.6:c.-11G>A MANE Select | ENSP00000291592.4:n.-11G>A | |
| ENST00000291592.5:c.-11G>A | ENSP00000291592.4:n.-11G>A | |
| NM_030891.4:c.-11G>A | NP_112153.1:n.-11G>A | |
| NM_030891.5:c.-11G>A | NP_112153.1:n.-11G>A | |
| NM_030891.6:c.-11G>A MANE Select | NP_112153.1:n.-11G>A |