Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2283456G>A , CM000678.2:g.2283456G>A | GRCh38 |
| NC_000016.9:g.2333457G>A , CM000678.1:g.2333457G>A | GRCh37 |
| NC_000016.8:g.2273458G>A | NCBI36 |
| NG_011790.1:g.62291C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.3863-98C>T MANE Select | NP_001080.2:n.3863-98C>T |
| ENST00000301732.10:c.3863-98C>T MANE Select | ENSP00000301732.5:n.3863-98C>T |
| NM_001089.2:c.3863-98C>T | NP_001080.2:n.3863-98C>T |
| ENST00000301732.9:c.3863-98C>T | ENSP00000301732.5:n.3863-98C>T |
| ENST00000382381.7:c.3689-98C>T | ENSP00000371818.3:n.3689-98C>T |
| ENST00000566200.1:n.286C>T | |
| ENST00000569062.1:n.517C>T |