Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23222598A>T , CM000670.2:g.23222598A>T | GRCh38 |
| NC_000008.10:g.23080111A>T , CM000670.1:g.23080111A>T | GRCh37 |
| NC_000008.9:g.23136056A>T | NCBI36 |
| NG_032107.1:g.7570T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000221132.8:c.306+2158T>A MANE Select | ENSP00000221132.3:n.306+2158T>A | |
| ENST00000221132.7:c.306+2158T>A | ENSP00000221132.3:n.306+2158T>A | |
| ENST00000524158.5:c.-301+1835T>A | ENSP00000428884.1:n.-301+1835T>A | |
| ENST00000613472.1:c.31+2433T>A | ENSP00000480778.1:n.31+2433T>A | |
| NM_003844.3:c.306+2158T>A | NP_003835.3:n.306+2158T>A | |
| NM_003844.4:c.306+2158T>A MANE Select | NP_003835.3:n.306+2158T>A |