Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115731201T= , CM000663.2:g.115731201T= | GRCh38 |
| NC_000001.10:g.116273822T= , CM000663.1:g.116273822T= | GRCh37 |
| NC_000001.9:g.116075345T= | NCBI36 |
| NG_008802.1:g.42605A= , LRG_404:g.42605A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.425+913A= | ENSP00000518226.1:n.425+913A= | |
| ENST00000261448.6:c.606+1700A= MANE Select | ENSP00000261448.5:n.606+1700A= | |
| ENST00000261448.5:c.606+1700A= | ENSP00000261448.5:n.606+1700A= | |
| ENST00000488931.1:n.122+913A= | ||
| NM_001232.3:c.606+1700A= , LRG_404t1:c.606+1700A= | NP_001223.2:n.606+1700A= | |
| NM_001232.4:c.606+1700A= MANE Select | NP_001223.2:n.606+1700A= |