Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2284275T>A , CM000678.2:g.2284275T>A | GRCh38 |
| NC_000016.9:g.2334276T>A , CM000678.1:g.2334276T>A | GRCh37 |
| NC_000016.8:g.2274277T>A | NCBI36 |
| NG_011790.1:g.61472A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.3862+4A>T MANE Select | NP_001080.2:n.3862+4A>T |
| ENST00000301732.10:c.3862+4A>T MANE Select | ENSP00000301732.5:n.3862+4A>T |
| NM_001089.2:c.3862+4A>T | NP_001080.2:n.3862+4A>T |
| ENST00000301732.9:c.3862+4A>T | ENSP00000301732.5:n.3862+4A>T |
| ENST00000382381.7:c.3688+4A>T | ENSP00000371818.3:n.3688+4A>T |