Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115738490C>T , CM000663.2:g.115738490C>T | GRCh38 |
| NC_000001.10:g.116281111C>T , CM000663.1:g.116281111C>T | GRCh37 |
| NC_000001.9:g.116082634C>T | NCBI36 |
| NG_008802.1:g.35316G>A , LRG_404:g.35316G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000488931.2:c.145-155G>A | ENSP00000518226.1:n.145-155G>A | |
| ENST00000261448.6:c.421-155G>A MANE Select | ENSP00000261448.5:n.421-155G>A | |
| ENST00000261448.5:c.421-155G>A | ENSP00000261448.5:n.421-155G>A | |
| NM_001232.3:c.421-155G>A , LRG_404t1:c.421-155G>A | NP_001223.2:n.421-155G>A | |
| NM_001232.4:c.421-155G>A MANE Select | NP_001223.2:n.421-155G>A |