Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30314254A>T , CM000672.2:g.30314254A>T | GRCh38 |
| NC_000010.10:g.30603183A>T , CM000672.1:g.30603183A>T | GRCh37 |
| NC_000010.9:g.30643189A>T | NCBI36 |
| NG_028096.1:g.40085T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.1387-283T>A MANE Select | ENSP00000263063.3:n.1387-283T>A | |
| ENST00000263063.8:c.1387-283T>A | ENSP00000263063.3:n.1387-283T>A | |
| ENST00000488290.5:n.3142-283T>A | ||
| NM_018109.3:c.1387-283T>A | NP_060579.3:n.1387-283T>A | |
| NM_018109.4:c.1387-283T>A MANE Select | NP_060579.3:n.1387-283T>A |