Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115033279T= , CM000663.2:g.115033279T= | GRCh38 |
| NC_000001.10:g.115575900T= , CM000663.1:g.115575900T= | GRCh37 |
| NC_000001.9:g.115377423T= | NCBI36 |
| NG_015891.1:g.8486T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256592.3:c.-1-83T= MANE Select | ENSP00000256592.1:n.-1-83T= | |
| ENST00000256592.2:c.-1-83T= | ENSP00000256592.1:n.-1-83T= | |
| NM_000549.4:c.-1-83T= | NP_000540.2:n.-1-83T= | |
| NM_000549.5:c.-1-83T= MANE Select | NP_000540.2:n.-1-83T= |