Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891490T>C , CM000673.2:g.128891490T>C | GRCh38 |
| NC_000011.9:g.128761385T>C , CM000673.1:g.128761385T>C | GRCh37 |
| NC_000011.8:g.128266595T>C | NCBI36 |
| NG_023406.2:g.5073T>C , LRG_333:g.5073T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-242T>C MANE Select | ENSP00000433295.1:n.-242T>C | |
| ENST00000338350.4:c.-331T>C | ENSP00000339960.4:n.-331T>C | |
| ENST00000529694.5:c.-242T>C | ENSP00000433295.1:n.-242T>C | |
| NM_000890.3:c.-242T>C , LRG_333t1:c.-242T>C | NP_000881.3:n.-242T>C | |
| NM_000890.4:c.-242T>C | NP_000881.3:n.-242T>C | |
| NM_001354169.1:c.-331T>C | NP_001341098.1:n.-331T>C | |
| NM_000890.5:c.-242T>C MANE Select | NP_000881.3:n.-242T>C | |
| NM_001354169.2:c.-331T>C | NP_001341098.1:n.-331T>C |