Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42900814A= , CM000679.2:g.42900814A= | GRCh38 |
| NC_000017.10:g.41052831A= , CM000679.1:g.41052831A= | GRCh37 |
| NC_000017.9:g.38306357A= | NCBI36 |
| NG_011808.1:g.5017A= , LRG_147:g.5017A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.-63A= MANE Select | ENSP00000253801.1:n.-63A= | |
| ENST00000253801.6:c.-63A= | ENSP00000253801.1:n.-63A= | |
| ENST00000585489.1:c.-63A= | ENSP00000466202.1:n.-63A= | |
| ENST00000588481.1:n.3A= | ||
| ENST00000592383.5:c.-63A= | ENSP00000465958.1:n.-63A= | |
| NM_000151.3:c.-63A= | NP_000142.2:n.-63A= | |
| NM_001270397.1:c.-63A= | NP_001257326.1:n.-63A= | |
| NM_000151.4:c.-63A= MANE Select | NP_000142.2:n.-63A= | |
| NM_001270397.2:c.-63A= | NP_001257326.1:n.-63A= |