Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114707204T= , CM000663.2:g.114707204T= | GRCh38 |
| NC_000001.10:g.115249825T= , CM000663.1:g.115249825T= | GRCh37 |
| NC_000001.9:g.115051348T= | NCBI36 |
| NG_007572.1:g.14691A= , LRG_92:g.14691A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.*890A= MANE Select | ENSP00000358548.4:n.*890A= | |
| ENST00000369535.4:c.*890A= | ENSP00000358548.4:n.*890A= | |
| NM_002524.4:c.*890A= | NP_002515.1:n.*890A= | |
| NM_002524.5:c.*890A= MANE Select | NP_002515.1:n.*890A= |