Linked Data
gnomAD v4:
11-128891513-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891513C>T , CM000673.2:g.128891513C>T | GRCh38 |
| NC_000011.9:g.128761408C>T , CM000673.1:g.128761408C>T | GRCh37 |
| NC_000011.8:g.128266618C>T | NCBI36 |
| NG_023406.2:g.5096C>T , LRG_333:g.5096C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-219C>T MANE Select | ENSP00000433295.1:n.-219C>T | |
| ENST00000338350.4:c.-308C>T | ENSP00000339960.4:n.-308C>T | |
| ENST00000529694.5:c.-219C>T | ENSP00000433295.1:n.-219C>T | |
| NM_000890.3:c.-219C>T , LRG_333t1:c.-219C>T | NP_000881.3:n.-219C>T | |
| NM_000890.4:c.-219C>T | NP_000881.3:n.-219C>T | |
| NM_001354169.1:c.-308C>T | NP_001341098.1:n.-308C>T | |
| NM_000890.5:c.-219C>T MANE Select | NP_000881.3:n.-219C>T | |
| NM_001354169.2:c.-308C>T | NP_001341098.1:n.-308C>T |