Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43169098A>T , CM000683.2:g.43169098A>T | GRCh38 |
| NG_009823.1:g.5068A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.-2A>T MANE Select | ENSP00000291554.2:n.-2A>T | |
| ENST00000482775.1:n.12A>T | ||
| NM_000394.3:c.-2A>T | NP_000385.1:n.-2A>T | |
| XR_001755073.1:n.647+1939T>A | ||
| NM_000394.4:c.-2A>T MANE Select | NP_000385.1:n.-2A>T |