Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114706981T= , CM000663.2:g.114706981T= | GRCh38 |
| NC_000001.10:g.115249602T= , CM000663.1:g.115249602T= | GRCh37 |
| NC_000001.9:g.115051125T= | NCBI36 |
| NG_007572.1:g.14914A= , LRG_92:g.14914A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*1113A= MANE Select | ENSP00000358548.4:n.*1113A= | |
| ENST00000369535.4:c.*1113A= | ENSP00000358548.4:n.*1113A= | |
| NM_002524.4:c.*1113A= | NP_002515.1:n.*1113A= | |
| NM_002524.5:c.*1113A= MANE Select | NP_002515.1:n.*1113A= |