Linked Data
gnomAD v4:
11-128891648-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891648G>A , CM000673.2:g.128891648G>A | GRCh38 |
| NC_000011.9:g.128761543G>A , CM000673.1:g.128761543G>A | GRCh37 |
| NC_000011.8:g.128266753G>A | NCBI36 |
| NG_023406.2:g.5231G>A , LRG_333:g.5231G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-84G>A MANE Select | ENSP00000433295.1:n.-84G>A | |
| ENST00000338350.4:c.-173G>A | ENSP00000339960.4:n.-173G>A | |
| ENST00000529694.5:c.-84G>A | ENSP00000433295.1:n.-84G>A | |
| NM_000890.3:c.-84G>A , LRG_333t1:c.-84G>A | NP_000881.3:n.-84G>A | |
| NM_000890.4:c.-84G>A | NP_000881.3:n.-84G>A | |
| NM_001354169.1:c.-173G>A | NP_001341098.1:n.-173G>A | |
| NM_000890.5:c.-84G>A MANE Select | NP_000881.3:n.-84G>A | |
| NM_001354169.2:c.-173G>A | NP_001341098.1:n.-173G>A |