Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891396G>T , CM000673.2:g.128891396G>T | GRCh38 |
| NC_000011.9:g.128761291G>T , CM000673.1:g.128761291G>T | GRCh37 |
| NC_000011.8:g.128266501G>T | NCBI36 |
| NG_023406.2:g.4979G>T , LRG_333:g.4979G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-336G>T MANE Select | ENSP00000433295.1:n.-336G>T | |
| ENST00000529694.5:c.-336G>T | ENSP00000433295.1:n.-336G>T | |
| NM_000890.4:c.-336G>T | NP_000881.3:n.-336G>T | |
| NM_001354169.1:c.-425G>T | NP_001341098.1:n.-425G>T | |
| NM_000890.5:c.-336G>T MANE Select | NP_000881.3:n.-336G>T | |
| NM_001354169.2:c.-425G>T | NP_001341098.1:n.-425G>T |